Gene ontology: date: 05:12:2007 15:33 Revision: 5.589
For annotation versions, see below.
Locate OMIM disorder using this index
A B C D E F G H I J K L M N O P R S T U V W X Y Z 2 3


A
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
ABCD syndrome600501Graph: ABCD syndromeMouseHumanRatXXXXXXXXXX
ACTH deficiency201400Graph: ACTH deficiencyMouseHumanRatXFlyXXXXXXXX
ADULT syndrome103285Graph: ADULT syndromeMouseHumanRatXXXXXXXXXX
AICA-ribosiduria due to ATIC deficiency608688Graph: AICA-ribosiduria due to ATIC deficiencyXHumanRatXXXXXXXYeastXX
AIDS, rapid progression to609423Graph: AIDS, rapid progression toMouseHumanRatXXXXXXXXXX
ARC syndrome208085Graph: ARC syndromeXXXXXXXXXXYeastXX
Abetalipoproteinemia200100Graph: AbetalipoproteinemiaMouseXXXXXXZfinXXXXX
Acampomelic campolelic dysplasia114290Graph: Acampomelic campolelic dysplasiaMouseHumanXXXXXZfinXXXXX
Achalasia-addisonianism-alacrimia syndrome231550Graph: Achalasia-addisonianism-alacrimia syndromeXHumanXXXXXXXXXXX
Acheiropody200500Graph: AcheiropodyMouseXXXXXXXXXXXX
Achondrogenesis Ib600972Graph: Achondrogenesis IbXHumanRatXXXXXXXXXX
Achondrogenesis-hypochondrogenesis, type II200610Graph: Achondrogenesis-hypochondrogenesis, type IIMouseHumanRatXXXXXXXXXX
Achondroplasia100800Graph: AchondroplasiaMouseHumanXWormXXXXXXXXX
Achromatopsia-2216900Graph: Achromatopsia-2MouseHumanXXXXXXXXXXX
Achromatopsia-3262300Graph: Achromatopsia-3MouseHumanXXXXXXXXXXX
Acrocallosal syndrome200990Graph: Acrocallosal syndromeMouseHumanRatXFlyXXXXXYeastXX
Acrocapitofemoral dysplasia607778Graph: Acrocapitofemoral dysplasiaMouseXXWormXXXXXXXXX
Acrodermatitis enteropathica201100Graph: Acrodermatitis enteropathicaMouseXXXXXXXXXXXX
Acrokeratosis verruciformis101900Graph: Acrokeratosis verruciformisMouseHumanRatWormXXXXXXXXX
Acromegaly102200Graph: AcromegalyMouseXRatWormXXXXXXXXX
Acromesomelic dysplasia, Hunter-Thompson type201250Graph: Acromesomelic dysplasia, Hunter-Thompson typeMouseHumanXXXXXXXXXXX
Acromesomelic dysplasia, Maroteaux type602875Graph: Acromesomelic dysplasia, Maroteaux typeMouseHumanXXXXXXXXXXX
Acyl-CoA dehydrogenase, medium chain, deficiency of201450Graph: Acyl-CoA dehydrogenase, medium chain, deficiency ofMouseHumanRatXXXXXXXXXX
Acyl-CoA dehydrogenase, short-chain, deficiency of201470Graph: Acyl-CoA dehydrogenase, short-chain, deficiency ofMouseHumanRatXXXXXXXXXX
Adenocarcinoma of lung, response to tyrosine kinase inhibitor in211980Graph: Adenocarcinoma of lung, response to tyrosine kinase inhibitor inMouseHumanRatWormXDictyXXXXYeastXX
Adenocarcinoma of lung, somatic211980Graph: Adenocarcinoma of lung, somaticMouseHumanRatWormXDictyXXXXYeastXX
Adenocarcinoma, ovarian, somatic604370Graph: Adenocarcinoma, ovarian, somaticMouseHumanRatWormXDictyXXXXXXX
Adenomas, multiple colorectal608456Graph: Adenomas, multiple colorectalMouseHumanRatXXXXXXXXXX
Adenomas, salivary gland pleomorphic181030Graph: Adenomas, salivary gland pleomorphicXHumanXXXXXXXTairXXX
Adenylosuccinase deficiency103050Graph: Adenylosuccinase deficiencyXHumanXXXXXXXXYeastXX
Adrenal cortical carcinoma202300Graph: Adrenal cortical carcinomaMouseHumanRatXXXXXXXXXX
Adrenal hyperplasia, congenital, due to combined P450C17 and P450C21 deficiency201750Graph: Adrenal hyperplasia, congenital, due to combined P450C17 and P450C21 deficiencyMouseHumanXXXXXXXXYeastXX
Adrenal hypoplasia, congenital, with hypogonadotropic hypogonadism300200Graph: Adrenal hypoplasia, congenital, with hypogonadotropic hypogonadismMouseXXXXXXXXXXXX
Adrenocorticotropic hormone deficiency201400Graph: Adrenocorticotropic hormone deficiencyMouseHumanRatXFlyXXXXXXXX
Adrenoleukodystrophy300100Graph: AdrenoleukodystrophyXHumanXXXXXXXXYeastXX
Adrenoleukodystrophy, neonatal202370Graph: Adrenoleukodystrophy, neonatalMouseHumanXWormXXXXXXYeastXX
Adrenomyeloneuropathy300100Graph: AdrenomyeloneuropathyXHumanXXXXXXXXYeastXX
Adult i phenotype with congenital cataract110800Graph: Adult i phenotype with congenital cataractMouseHumanXXXXXXXXXXX
Adult i phenotype without cataract110800Graph: Adult i phenotype without cataractMouseHumanXXXXXXXXXXX
Advanced sleep phase syndrome, familial604348Graph: Advanced sleep phase syndrome, familialMouseHumanRatXXXXXXXXXX
Afibrinogenemia, congenital202400Graph: Afibrinogenemia, congenitalXHumanRatXXXXXXXXXX
Agammaglobulinemia601495Graph: AgammaglobulinemiaMouseHumanXXXXXXXXXXX
Agammaglobulinemia, autosomal recessive601495Graph: Agammaglobulinemia, autosomal recessiveMouseHumanXXXXXXXXXXX
Agammaglobulinemia, non-Bruton type601495Graph: Agammaglobulinemia, non-Bruton typeMouseHumanXXXXXXXXXXX
Agenesis of the corpus callosum with peripheral neuropathy218000Graph: Agenesis of the corpus callosum with peripheral neuropathyMouseHumanXXXXXXXXXXX
Alagille syndrome118450Graph: Alagille syndromeMouseHumanRatXXXXZfinXXXXX
Albinism, brown203290Graph: Albinism, brownMouseXXXXXXXXXXXX
Albinism, oculocutaneous, type IA203100Graph: Albinism, oculocutaneous, type IAMouseHumanXXXXXXXXXXX
Albinism, oculocutaneous, type IB606952Graph: Albinism, oculocutaneous, type IBMouseHumanXXXXXXXXXXX
Albinism, rufous278400Graph: Albinism, rufousMouseXXXXXXXXXXXX
Aldosteronism, glucocorticoid-remediable103900Graph: Aldosteronism, glucocorticoid-remediableXHumanRatXXXXXXXXXX
Alexander disease203450Graph: Alexander diseaseMouseHumanRatWormXXXZfinXXXXX
Alkaptonuria203500Graph: AlkaptonuriaXHumanXXXXXXXXXXX
Allan-Herndon-Dudley syndrome300523Graph: Allan-Herndon-Dudley syndromeXHumanXXXXXXXXYeastXX
Alopecia universalis203655Graph: Alopecia universalisXXXXXXXXXXXXX
Alpers syndrome203700Graph: Alpers syndromeMouseHumanRatXXXXXXXYeastXX
Alpha-methylacetoacetic aciduria203750Graph: Alpha-methylacetoacetic aciduriaMouseHumanRatXXXXXXXYeastXX
Alpha-thalassemia myelodysplasia syndrome, somatic300448Graph: Alpha-thalassemia myelodysplasia syndrome, somaticMouseHumanRatWormXXXXXXXXX
Alpha-thalassemia/mental retardation syndrome301040Graph: Alpha-thalassemia/mental retardation syndromeMouseHumanRatWormXXXXXXXXX
Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity609889Graph: Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunityMouseHumanXXXXXXXXXXX
Alport syndrome301050Graph: Alport syndromeMouseHumanXWormXXXXXXXXX
Alport syndrome, autosomal recessive203780Graph: Alport syndrome, autosomal recessiveMouseHumanXXXXXXXXXXX
Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis300194Graph: Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosisXXXXXXXXXXXXX
Alstrom syndrome203800Graph: Alstrom syndromeMouseHumanXXXXXXXXXXX
Alternating hemiplegia of childhood104290Graph: Alternating hemiplegia of childhoodMouseXRatWormXXXZfinXXXXX
Alveolar soft-part sarcoma606243Graph: Alveolar soft-part sarcomaMouseXXXXXXXXXXXX
Alzheimer disease, type 3607822Graph: Alzheimer disease, type 3MouseHumanRatXXXXXXXXXX
Alzheimer disease, type 3, with spastic paraparesis and apraxia607822Graph: Alzheimer disease, type 3, with spastic paraparesis and apraxiaMouseHumanRatXXXXXXXXXX
Alzheimer disease, type 3, with spastic paraparesis and unusual plaques607822Graph: Alzheimer disease, type 3, with spastic paraparesis and unusual plaquesMouseHumanRatXXXXXXXXXX
Alzheimer disease-2104310Graph: Alzheimer disease-2MouseHumanRatXXXXXXXXXX
Alzheimer disease-4606889Graph: Alzheimer disease-4MouseHumanRatXXXXXXXXXX
Amelogenesis imperfecta 2, hypoplastic local104500Graph: Amelogenesis imperfecta 2, hypoplastic localXXXXXXXXXXXXX
Amelogenesis imperfecta, hypomaturation-hypoplastic type, with taurodontism104510Graph: Amelogenesis imperfecta, hypomaturation-hypoplastic type, with taurodontismXHumanXWormXXXZfinXXXXX
Amelogenesis imperfecta, hypoplastic, and openbite malocclusion608563Graph: Amelogenesis imperfecta, hypoplastic, and openbite malocclusionXXXXXXXXXXXXX
Amelogenesis imperfecta, hypoplastic/hypomaturation type301200Graph: Amelogenesis imperfecta, hypoplastic/hypomaturation typeMouseXRatXXXXXXXXXX
Amyloidosis, Finnish type105120Graph: Amyloidosis, Finnish typeMouseHumanRatXXXXXXXXXX
Amyloidosis, cerebroarterial, Iowa type605714Graph: Amyloidosis, cerebroarterial, Iowa typeMouseHumanRatXXXXXXXXXX
Amyloidosis, hereditary renal105200Graph: Amyloidosis, hereditary renalMouseHumanXXXXXZfinXXXXX
Amyloidosis, renal105200Graph: Amyloidosis, renalMouseHumanXXXXXZfinXXXXX
Amyotrophic lateral sclerosis 8608627Graph: Amyotrophic lateral sclerosis 8XHumanXXXXXXXXYeastXX
Amyotrophic lateral sclerosis, due to SOD1 deficiency105400Graph: Amyotrophic lateral sclerosis, due to SOD1 deficiencyMouseHumanRatXXXXXXXYeastXX
Amyotrophic lateral sclerosis, juvenile205100Graph: Amyotrophic lateral sclerosis, juvenileMouseHumanXXXXXXXXXXX
Anderson disease607689Graph: Anderson diseaseXXXXXXXXXXYeastXX
Androgen insensitivity300068Graph: Androgen insensitivityMouseHumanRatXXXXXXXXXX
Anemia, Diamond-Blackfan105650Graph: Anemia, Diamond-BlackfanXHumanXWormXXXXXXYeastXX
Anemia, congenital dyserythropoietic, type I224120Graph: Anemia, congenital dyserythropoietic, type IMouseXXXXXXXXXXXX
Anemia, hemolytic, Rh-null, regulator type268150Graph: Anemia, hemolytic, Rh-null, regulator typeXHumanXWormXDictyXXRiceXYeastXX
Anemia, hemolytic, due to UMPH1 deficiency266120Graph: Anemia, hemolytic, due to UMPH1 deficiencyXHumanXXXXXXXXXXX
Anemia, sideroblastic, with ataxia301310Graph: Anemia, sideroblastic, with ataxiaMouseHumanXXXXXXXXYeastXX
Angelman syndrome105830Graph: Angelman syndromeMouseHumanXXXXXXXXYeastXX
Angioedema, hereditary106100Graph: Angioedema, hereditaryXHumanXXXXXXXXXXX
Aniridia, type II106210Graph: Aniridia, type IIMouseHumanRatWormXXChickenXXXYeastXX
Anophthalmia 3206900Graph: Anophthalmia 3MouseXXXXXXXXXXXX
Anterior segment mesenchymal dysgenesis107250Graph: Anterior segment mesenchymal dysgenesisMouseHumanXXXXXXXXYeastXX
Anterior segment mesenchymal dysgenesis and cataract107250Graph: Anterior segment mesenchymal dysgenesis and cataractMouseHumanXXXXXXXXYeastXX
Antley-Bixler syndrome-like with disordered steroidogenesis201750Graph: Antley-Bixler syndrome-like with disordered steroidogenesisMouseHumanXXXXXXXXYeastXX
Anxiety-related personality traits607834Graph: Anxiety-related personality traitsXHumanRatXXXXXXXXXX
Aortic aneurysm, familial thoracic 3608967Graph: Aortic aneurysm, familial thoracic 3MouseHumanRatXXXXXXXXXX
Apert syndrome101200Graph: Apert syndromeMouseXXWormXXXXXXXXX
Aplastic anemia609135Graph: Aplastic anemiaMouseHumanRatXXXXXXXXXX
Argininemia207800Graph: ArgininemiaMouseHumanRatXXXXXXXYeastXX
Argininosuccinic aciduria207900Graph: Argininosuccinic aciduriaXHumanXXXXXXXXYeastXX
Aromatic L-amino acid decarboxylase deficiency608643Graph: Aromatic L-amino acid decarboxylase deficiencyXHumanRatXXXXXXXXXX
Arrhythmogenic right ventricular dysplasia 2600996Graph: Arrhythmogenic right ventricular dysplasia 2XHumanXWormXXXXXXXXX
Arrhythmogenic right ventricular dysplasia 8607450Graph: Arrhythmogenic right ventricular dysplasia 8XHumanXXXXXXXXXXX
Arrhythmogenic right ventricular dysplasia-5604400Graph: Arrhythmogenic right ventricular dysplasia-5XXRatWormXXXXXXYeastXX
Arterial calcification, generalized, of infancy208000Graph: Arterial calcification, generalized, of infancyMouseHumanXXXXXXXXXXX
Arthrogryposis multiplex congenita, distal, type 1108120Graph: Arthrogryposis multiplex congenita, distal, type 1XHumanRatWormXXXXXXYeastXX
Arthrogryposis multiplex congenita, distal, type 2B601680Graph: Arthrogryposis multiplex congenita, distal, type 2BXXXWormXXXXXXYeastXX
Arthropathy, progressive pseudorheumatoid, of childhood208230Graph: Arthropathy, progressive pseudorheumatoid, of childhoodXHumanXXFlyXXXXXXXX
Arthyrgryposis, distal, type 2B601680Graph: Arthyrgryposis, distal, type 2BXXXWormXXXXXXYeastXX
Ataxia with isolated vitamin E deficiency277460Graph: Ataxia with isolated vitamin E deficiencyMouseHumanRatXXXXXXXXXX
Ataxia, cerebellar, Cayman type601238Graph: Ataxia, cerebellar, Cayman typeXXXXXXXXXXXXX
Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia208920Graph: Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemiaMouseHumanXXXXXXXXYeastXX
Ataxia-ocular apraxia-2606002Graph: Ataxia-ocular apraxia-2XXXXXXXXXXXXX
Ataxia-telangiectasia208900Graph: Ataxia-telangiectasiaMouseHumanXXXXXXXXXXX
Ataxia-telangiectasia-like disorder604391Graph: Ataxia-telangiectasia-like disorderMouseHumanRatXXXXXXXYeastXX
Atelosteogenesis II256050Graph: Atelosteogenesis IIXHumanRatXXXXXXXXXX
Atelostogenesis, type I108720Graph: Atelostogenesis, type IMouseHumanXXXDictyXXXXXXX
Atopy147050Graph: AtopyMouseHumanXXXXXXXXXXX
Atransferrinemia209300Graph: AtransferrinemiaXHumanRatXXXXXXXXXX
Atrial fibrillation, familial607554Graph: Atrial fibrillation, familialMouseHumanRatXXXXXXXXXX
Atrial septal defect with atrioventricular conduction defects108900Graph: Atrial septal defect with atrioventricular conduction defectsMouseXRatWormXXXXXXXXX
Atrial septal defect-2607941Graph: Atrial septal defect-2MouseHumanRatWormXXXXXXXXX
Atrichia with papular lesions209500Graph: Atrichia with papular lesionsXXXXXXXXXXXXX
Atrioventricular septal defect600309Graph: Atrioventricular septal defectMouseHumanRatXXXXZfinXXXXX
Atrioventricular septal defect, partial, with heterotaxy syndrome606217Graph: Atrioventricular septal defect, partial, with heterotaxy syndromeXXXXXXXXXXXXX
Autoimmune lymphoproliferative syndrome, type IA601859Graph: Autoimmune lymphoproliferative syndrome, type IAMouseHumanRatXXXXXXXXXX
Autoimmune lymphoproliferative syndrome, type II603909Graph: Autoimmune lymphoproliferative syndrome, type IIXHumanXXXXXXXXXXX
Autoimmune lymphoproliferative syndrome, type IIB607271Graph: Autoimmune lymphoproliferative syndrome, type IIBMouseHumanRatXXXXXXXXXX
Autoimmune polyglandular disease, type I240300Graph: Autoimmune polyglandular disease, type IXHumanXXXXXXXXXXX
Azoospermia415000Graph: AzoospermiaMouseHumanRatXXXXXXXXXX

B
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
BCG and salmonella infection, disseminated209950Graph: BCG and salmonella infection, disseminatedMouseHumanRatXXXXXXXXXX
BCG infection, generalized familial209950Graph: BCG infection, generalized familialMouseHumanRatXXXXXXXXXX
Baller-Gerold syndrome218600Graph: Baller-Gerold syndromeXHumanXXXXXXXXXXX
Bannayan-Riley-Ruvalcaba syndrome153480Graph: Bannayan-Riley-Ruvalcaba syndromeMouseHumanRatWormXDictyXXXXXXX
Bannayan-Zonana syndrome153480Graph: Bannayan-Zonana syndromeMouseHumanRatWormXDictyXXXXXXX
Bardet-Biedl syndrome 1209900Graph: Bardet-Biedl syndrome 1MouseHumanRatXXXXXXXXXX
Bardet-Biedl syndrome 1, modifier of209900Graph: Bardet-Biedl syndrome 1, modifier ofMouseHumanRatXXXXXXXXXX
Bardet-Biedl syndrome 2209900Graph: Bardet-Biedl syndrome 2MouseHumanRatXXXXXXXXXX
Bardet-Biedl syndrome 3209900Graph: Bardet-Biedl syndrome 3MouseHumanRatXXXXXXXXXX
Bardet-Biedl syndrome 4209900Graph: Bardet-Biedl syndrome 4MouseHumanRatXXXXXXXXXX
Bardet-Biedl syndrome 5209900Graph: Bardet-Biedl syndrome 5MouseHumanRatXXXXXXXXXX
Bardet-Biedl syndrome 6209900Graph: Bardet-Biedl syndrome 6MouseHumanRatXXXXXXXXXX
Bardet-Biedl syndrome 7209900Graph: Bardet-Biedl syndrome 7MouseHumanRatXXXXXXXXXX
Bardet-Biedl syndrome 8209900Graph: Bardet-Biedl syndrome 8MouseHumanRatXXXXXXXXXX
Bare lymphocyte syndrome, type I604571Graph: Bare lymphocyte syndrome, type IMouseHumanRatXXXXXXXXXX
Bare lymphocyte syndrome, type I, due to TAP2 deficiency604571Graph: Bare lymphocyte syndrome, type I, due to TAP2 deficiencyMouseHumanRatXXXXXXXXXX
Bare lymphocyte syndrome, type II, complementation group A209920Graph: Bare lymphocyte syndrome, type II, complementation group AMouseHumanRatXXXXXXXXXX
Bare lymphocyte syndrome, type II, complementation group C209920Graph: Bare lymphocyte syndrome, type II, complementation group CMouseHumanRatXXXXXXXXXX
Bare lymphocyte syndrome, type II, complementation group D209920Graph: Bare lymphocyte syndrome, type II, complementation group DMouseHumanRatXXXXXXXXXX
Bare lymphocyte syndrome, type II, complementation group E209920Graph: Bare lymphocyte syndrome, type II, complementation group EMouseHumanRatXXXXXXXXXX
Bart-Pumphrey syndrome149200Graph: Bart-Pumphrey syndromeMouseHumanRatXXXXXXXXXX
Barth syndrome302060Graph: Barth syndromeXHumanXXXXXXXXYeastXX
Bartter syndrome, type 1601678Graph: Bartter syndrome, type 1XHumanXXXXXXXXXXX
Bartter syndrome, type 2241200Graph: Bartter syndrome, type 2XHumanXXXXXXXXXXX
Bartter syndrome, type 3607364Graph: Bartter syndrome, type 3MouseHumanRatXXXXXXXXXX
Bartter syndrome, type 4602522Graph: Bartter syndrome, type 4MouseHumanRatXXXXXXXXXX
Bartter syndrome, type 4, digenic602522Graph: Bartter syndrome, type 4, digenicMouseHumanRatXXXXXXXXXX
Basal cell carcinoma, somatic605462Graph: Basal cell carcinoma, somaticMouseHumanXWormXXXXXXXXX
Basal cell nevus syndrome109400Graph: Basal cell nevus syndromeMouseHumanXWormXXXXXXXXX
Basal ganglia disease, adult-onset606159Graph: Basal ganglia disease, adult-onsetXHumanXXXXXXXXXXX
Beare-Stevenson cutis gyrata syndrome123790Graph: Beare-Stevenson cutis gyrata syndromeMouseXXWormXXXXXXXXX
Becker muscular dystrophy300376Graph: Becker muscular dystrophyMouseHumanXXXXXZfinXXXXX
Becker muscular dystrophy modifier310200Graph: Becker muscular dystrophy modifierMouseHumanXWormXXXZfinXXXXX
Beckwith-Wiedemann syndrome130650Graph: Beckwith-Wiedemann syndromeMouseHumanXWormXXXZfinXXXXX
Bernard-Soulier syndrome, type A231200Graph: Bernard-Soulier syndrome, type AMouseHumanXXXXXXXXXXX
Bernard-Soulier syndrome, type C231200Graph: Bernard-Soulier syndrome, type CMouseHumanXXXXXXXXXXX
Bethlem myopathy158810Graph: Bethlem myopathyMouseHumanXXXXXXXXXXX
Birt-Hogg-Dube syndrome135150Graph: Birt-Hogg-Dube syndromeXXXXXXXXXXXXX
Bladder cancer109800Graph: Bladder cancerMouseHumanXWormXDictyXXXXXXX
Blau syndrome186580Graph: Blau syndromeMouseHumanXXXXXXXXXXX
Bleeding disorder due to P2RY12 defect609821Graph: Bleeding disorder due to P2RY12 defectMouseXRatXXXXXXXXXX
Blepharophimosis, epicanthus inversus, and ptosis, type 1110100Graph: Blepharophimosis, epicanthus inversus, and ptosis, type 1MouseXXXXXXXXXXXX
Blepharophimosis, epicanthus inversus, and ptosis, type 2110100Graph: Blepharophimosis, epicanthus inversus, and ptosis, type 2MouseXXXXXXXXXXXX
Bloom syndrome210900Graph: Bloom syndromeMouseHumanXXXXXXXXXXX
Blue-cone monochromacy303700Graph: Blue-cone monochromacyMouseHumanXXXXXXXXXXX
Borjeson-Forssman-Lehmann syndrome301900Graph: Borjeson-Forssman-Lehmann syndromeXXXXXXXXXXXXX
Bothnia retinal dystrophy607475Graph: Bothnia retinal dystrophyMouseHumanXXXXXXXXXXX
Brachydactyly, type A1112500Graph: Brachydactyly, type A1MouseXXWormXXXXXXXXX
Brachydactyly, type A2112600Graph: Brachydactyly, type A2MouseHumanXWormXXXXXXXXX
Brachydactyly, type B1113000Graph: Brachydactyly, type B1MouseHumanXWormXXXXXXXXX
Brachydactyly, type C113100Graph: Brachydactyly, type CMouseHumanXXXXXXXXXXX
Brachydactyly, type D113200Graph: Brachydactyly, type DMouseHumanXXXXXXXXXXX
Brachydactyly, type E113300Graph: Brachydactyly, type EMouseHumanXXXXXXXXXXX
Bradyopsia608415Graph: BradyopsiaMouseHumanRatXXXXXXXXXX
Branchiootorenal syndrome113650Graph: Branchiootorenal syndromeMouseHumanXXXXXXXXXXX
Branchiootorenal syndrome with cataract113650Graph: Branchiootorenal syndrome with cataractMouseHumanXXXXXXXXXXX
Breast cancer114480Graph: Breast cancerMouseHumanRatWormXDictyXXXXXXX
Breast cancer, early-onset114480Graph: Breast cancer, early-onsetMouseHumanRatWormXDictyXXXXXXX
Breast cancer, somatic114480Graph: Breast cancer, somaticMouseHumanRatWormXDictyXXXXXXX
Brody myopathy601003Graph: Brody myopathyMouseHumanRatWormXXXZfinXXXXX
Brugada syndrome601144Graph: Brugada syndromeXHumanRatXXXXXXXXXX
Burkitt lymphoma113970Graph: Burkitt lymphomaMouseHumanRatXXXXXXXXXX
Butterfly dystrophy, retinal169150Graph: Butterfly dystrophy, retinalXHumanXXXXXXXXXXX

C
OMIM disorder(s)OMIM_idComparisonGraphMouseHumanRatWormFlyDictyChickenZfinRiceTairYeastPombePfalc
CHILD syndrome308050Graph: CHILD syndromeMouseHumanXXXXXXXXYeastXX
CINCA syndrome607115Graph: CINCA syndromeXHumanXXXDictyXXXXXXX
CPT II deficiency, lethal neonatal608836Graph: CPT II deficiency, lethal neonatalMouseXRatXXXXXXXYeastXX
CPT deficiency, hepatic, type IA255120Graph: CPT deficiency, hepatic, type IAMouseHumanRatXXXXXXXXXX
CPT deficiency, hepatic, type II600649Graph: CPT deficiency, hepatic, type IIMouseXRatXXXXXXXYeastXX
CRASH syndrome303350Graph: CRASH syndromeMouseHumanXXXXXZfinXXXXX
Cafe-au-lait spots with glioma or leukemia114030Graph: Cafe-au-lait spots with glioma or leukemiaMouseHumanXXXXXXXXYeastXX
Caffey disease114000Graph: Caffey diseaseXHumanXXXXXXXXXXX
Calcinosis, tumoral211900Graph: Calcinosis, tumoralMouseXXXXXXXXXXXX
Campomelic dysplasia114290Graph: Campomelic dysplasiaMouseHumanXXXXXZfinXXXXX
Campomelic dysplasia with autosomal sex reversal114290Graph: Campomelic dysplasia with autosomal sex reversalMouseHumanXXXXXZfinXXXXX
Camptodactyly-arthropathy-coxa vara-pericarditis syndrome208250Graph: Camptodactyly-arthropathy-coxa vara-pericarditis syndromeXHumanXXXXXXXXXXX
Camurati-Engelmann disease131300Graph: Camurati-Engelmann diseaseMouseHumanRatXXXXXXXXXX
Canavan disease271900Graph: Canavan diseaseMouseHumanRatXXXXXXXXXX
Capillary malformation-arteriovenous malformation608354Graph: Capillary malformation-arteriovenous malformationMouseHumanXXXXXXXXXXX
Carbamoylphosphate synthetase I deficiency237300Graph: Carbamoylphosphate synthetase I deficiencyXHumanXXXXXXXXXXX
Carbohydrate-deficient glycoprotein syndrome, type I212065Graph: Carbohydrate-deficient glycoprotein syndrome, type IXHumanXXXXXXXXYeastPombeX
Carbohydrate-deficient glycoprotein syndrome, type II212066Graph: Carbohydrate-deficient glycoprotein syndrome, type IIMouseHumanXXXXXXXXXXX
Carbohydrate-deficient glycoprotein syndrome, type Ib602579Graph: Carbohydrate-deficient glycoprotein syndrome, type IbXHumanXXXXXXXXYeastXX
Carboxypeptidase N deficiency212070Graph: Carboxypeptidase N deficiencyMouseHumanRatXXXXXXXXXX
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency604377Graph: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiencyXHumanXXXXXXXXYeastXX
Cardiofaciocutaneous syndrome115150Graph: Cardiofaciocutaneous syndromeMouseHumanXWormXXXXXXXXX
Cardiomopathy, Familial hypertrophic, 8608751Graph: Cardiomopathy, Familial hypertrophic, 8XHumanXXXXXXXXXXX
Cardiomyopathy, X-linked dilated300069Graph: Cardiomyopathy, X-linked dilatedXHumanXXXXXXXXYeastXX
Cardiomyopathy, dilated115200Graph: Cardiomyopathy, dilatedMouseHumanRatWormXXXXXXXXX
Cardiomyopathy, dilated, 1A115200Graph: Cardiomyopathy, dilated, 1AMouseHumanRatWormXXXXXXXXX
Cardiomyopathy, dilated, 1D601494Graph: Cardiomyopathy, dilated, 1DMouseHumanRatWormXXXZfinXXYeastXX
Cardiomyopathy, dilated, 1E601154Graph: Cardiomyopathy, dilated, 1EXHumanRatXXXXXXXXXX
Cardiomyopathy, dilated, 1G604145Graph: Cardiomyopathy, dilated, 1GMouseHumanRatWormXXXXXXXXPfalc
Cardiomyopathy, dilated, 1I604765Graph: Cardiomyopathy, dilated, 1IMouseHumanXXXXXXXXXXX
Cardiomyopathy, dilated, 1J605362Graph: Cardiomyopathy, dilated, 1JXHumanXXXXXXXXXXX
Cardiomyopathy, dilated, 1L606685Graph: Cardiomyopathy, dilated, 1LMouseHumanXXXXXXXXXXX
Cardiomyopathy, dilated, 1M607482Graph: Cardiomyopathy, dilated, 1MMouseHumanXXXXXXXXXXX
Cardiomyopathy, dilated, 1N607487Graph: Cardiomyopathy, dilated, 1NXHumanXXXXXXXXXXX
Cardiomyopathy, dilated, 1O608569Graph: Cardiomyopathy, dilated, 1OXHumanRatXXXXXXXXXX
Cardiomyopathy, dilated, X-linked302045Graph: Cardiomyopathy, dilated, X-linkedMouseHumanXXXXXZfinXXXXX
Cardiomyopathy, familial hypertrophic192600Graph: Cardiomyopathy, familial hypertrophicMouseHumanRatWormXDictyXXRiceXYeastPombeX
Cardiomyopathy, familial hypertrophic, 1192600Graph: Cardiomyopathy, familial hypertrophic, 1MouseHumanRatWormXDictyXXRiceXYeastPombeX
Cardiomyopathy, familial hypertrophic, 10608758Graph: Cardiomyopathy, familial hypertrophic, 10XHumanXWormXXXXXXXXX
Cardiomyopathy, familial hypertrophic, 2115195Graph: Cardiomyopathy, familial hypertrophic, 2MouseHumanRatWormXXXZfinXXYeastXX
Cardiomyopathy, familial hypertrophic, 3115196Graph: Cardiomyopathy, familial hypertrophic, 3XHumanRatWormXXXXXXYeastXX
Cardiomyopathy, familial hypertrophic, 4115197Graph: Cardiomyopathy, familial hypertrophic, 4MouseHumanXXXXXXXXXXX
Cardiomyopathy, familial restrictive115210Graph: Cardiomyopathy, familial restrictiveMouseHumanRatWormXXXXXXXXX
Cardiomyopathy, hypertrophic, mid-left ventricular chamber type608758Graph: Cardiomyopathy, hypertrophic, mid-left ventricular chamber typeXHumanXWormXXXXXXXXX
Cardiomyopathy, hypertrophic, midventricular, digenic192600Graph: Cardiomyopathy, hypertrophic, midventricular, digenicMouseHumanRatWormXDictyXXRiceXYeastPombeX
Cardiomyopathy, hypertrophic, with WPW600858Graph: Cardiomyopathy, hypertrophic, with WPWMouseXXXXXXXXXYeastXX
Carney complex variant608837Graph: Carney complex variantXHumanXWormXDictyXXXXYeastPombeX
Carney complex, type 1160980Graph: Carney complex, type 1MouseHumanRatWormXDictyXXXXXXX
Carnitine deficiency, systemic primary212140Graph: Carnitine deficiency, systemic primaryXHumanRatXXXXXXXXXX
Cataract, Coppock-like604307Graph: Cataract, Coppock-likeMouseXXXXXXXXXXXX
Cataract, Marner type116800Graph: Cataract, Marner typeMouseHumanXWormXXXXXTairXXX
Cataract, cerulean, type 2601547Graph: Cataract, cerulean, type 2MouseHumanXXXXXXXXXXX
Cataract, congenital604219Graph: Cataract, congenitalMouseHumanXXXXXXXXYeastXX
Cataract, congenital zonular, with sutural opacities600881Graph: Cataract, congenital zonular, with sutural opacitiesMouseHumanXXXXXXXXXXX
Cataract, congenital, cerulean type, 3608983Graph: Cataract, congenital, cerulean type, 3MouseHumanXXXXXXXXXXX
Cataract, crystalline aculeiform115700Graph: Cataract, crystalline aculeiformMouseHumanXXXXXXXXXXX
Cataract, juvenile-onset604219Graph: Cataract, juvenile-onsetMouseHumanXXXXXXXXYeastXX
Cataract, lamellar116800Graph: Cataract, lamellarMouseHumanXWormXXXXXTairXXX
Cataract, polymorphic and lamellar604219Graph: Cataract, polymorphic and lamellarMouseHumanXXXXXXXXYeastXX
Cataract, sutural, with punctate and cerulean opacities607133Graph: Cataract, sutural, with punctate and cerulean opacitiesMouseHumanXXXXXXXXXXX
Cataract, zonular pulverulent-1116200Graph: Cataract, zonular pulverulent-1MouseHumanXXXXXXXXXXX
Cataract, zonular pulverulent-3601885Graph: Cataract, zonular pulverulent-3MouseHumanRatXXXXXXXXXX
Cavernous malformations of CNS and retina116860Graph: Cavernous malformations of CNS and retinaXHumanXXXXXXXXXXX
Central core disease117000Graph: Central core diseaseMouseHumanXWormXXXXXXXXX
Central hypoventilation syndrome209880Graph: Central hypoventilation syndromeMouseHumanRatXXXXZfinXXXXX
Central hypoventilation syndrome, congenital209880Graph: Central hypoventilation syndrome, congenitalMouseHumanRatXXXXZfinXXXXX
Cerebellar ataxia604290Graph: Cerebellar ataxiaXHumanRatXXXXXXXXXX
Cerebral amyloid angiopathy105150Graph: Cerebral amyloid angiopathyXHumanXXXXXXXXXXX
Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy125310Graph: Cerebral arteriopathy with subcortical infarcts and leukoencephalopathyMouseXRatXXXXXXXXXX
Cerebral cavernous malformations-1116860Graph: Cerebral cavernous malformations-1XHumanXXXXXXXXXXX
Cerebral cavernous malformations-2603284Graph: Cerebral cavernous malformations-2XXXXXXXXXXXXX
Cerebrooculofacioskeletal syndrome214150Graph: Cerebrooculofacioskeletal syndromeMouseHumanXXXXXXXXYeastXX
Cerebrotendinous xanthomatosis213700Graph: Cerebrotendinous xanthomatosisMouseHumanRatXXXXXXXXXX
Ceroid lipofuscinosis, neuronal 8600143Graph: Ceroid lipofuscinosis, neuronal 8XHumanXXXXXXXXXXX
Ceroid lipofuscinosis, neuronal-1, infantile256730Graph: Ceroid lipofuscinosis, neuronal-1, infantileMouseHumanRatXXXXXXXXXX
Ceroid-lipofuscinosis, neuronal 2, classic late infantile204500Graph: Ceroid-lipofuscinosis, neuronal 2, classic late infantileXXXXXXXXXXXXX
Ceroid-lipofuscinosis, neuronal-3, juvenile204200Graph: Ceroid-lipofuscinosis, neuronal-3, juvenileXHumanXWormXXXXXXYeastXX
Ceroid-lipofuscinosis, neuronal-5, variant late infantile256731Graph: Ceroid-lipofuscinosis, neuronal-5, variant late infantileMouseHumanXXXXXXXXXXX
Ceroid-lipofuscinosis, neuronal-6, variant late infantile601780Graph: Ceroid-lipofuscinosis, neuronal-6, variant late infantileXXXXXXXXXXXXX
Cervical cancer, somatic603956Graph: Cervical cancer, somaticMouseHumanXWormXXXXXXXXX
Chanarin-Dorfman syndrome275630Graph: Chanarin-Dorfman syndromeMouseXXXXXXXXXYeastXX
Char syndrome169100Graph: Char syndromeMouseHumanXXXXXXXXXXX
Charcot-Marie-Tooth disease, axonal, type 2F606595Graph: Charcot-Marie-Tooth disease, axonal, type 2FMouseHumanXXXXXXXXXXX
Charcot-Marie-Tooth disease, dominant intermediate 3607791Graph: Charcot-Marie-Tooth disease, dominant intermediate 3MouseHumanXXXXXXXXXXX
Charcot-Marie-Tooth disease, mixed axonal and demyelinating type214400Graph: Charcot-Marie-Tooth disease, mixed axonal and demyelinating typeXXXXXXXXXXXXX
Charcot-Marie-Tooth disease, type 1A118220Graph: Charcot-Marie-Tooth disease, type 1AXHumanRatXXXXXXXXXX
Charcot-Marie-Tooth disease, type 1B118200Graph: Charcot-Marie-Tooth disease, type 1BMouseHumanXXXXXXXXXXX
Charcot-Marie-Tooth disease, type 1C601098Graph: Charcot-Marie-Tooth disease, type 1CMouseHumanXXXXXXXXXXX
Charcot-Marie-Tooth disease, type 1D607678Graph: Charcot-Marie-Tooth disease, type 1DMouseHumanRatXXXXXXXYeastXX
Charcot-Marie-Tooth disease, type 1E118300Graph: Charcot-Marie-Tooth disease, type 1EXHumanRatXXXXXXXXXX
Charcot-Marie-Tooth disease, type 1F607734Graph: Charcot-Marie-Tooth disease, type 1FMouseHumanRatXXXXXXXXXX
Charcot-Marie-Tooth disease, type 2A1118210Graph: Charcot-Marie-Tooth disease, type 2A1MouseHumanXWormXXXXXXXXX
Charcot-Marie-Tooth disease, type 2A2609260Graph: Charcot-Marie-Tooth disease, type 2A2MouseHumanXWormXXXXXXXXX
Charcot-Marie-Tooth disease, type 2B600882Graph: Charcot-Marie-Tooth disease, type 2BMouseHumanRatWormXXXXXXYeastXX
Charcot-Marie-Tooth disease, type 2D601472Graph: Charcot-Marie-Tooth disease, type 2DMouseHumanXWormXXXXXXYeastXX
Charcot-Marie-Tooth disease, type 2E607684Graph: Charcot-Marie-Tooth disease, type 2EMouseHumanRatXXXXXXXXXX
Charcot-Marie-Tooth disease, type 2G607706Graph: Charcot-Marie-Tooth disease, type 2GXXXXXXXXXXXXX
Charcot-Marie-Tooth disease, type 2I607677Graph: Charcot-Marie-Tooth disease, type 2IMouseHumanXXXXXXXXXXX
Charcot-Marie-Tooth disease, type 2J607736Graph: Charcot-Marie-Tooth disease, type 2JMouseHumanXXXXXXXXXXX
Charcot-Marie-Tooth disease, type 2K607831Graph: Charcot-Marie-Tooth disease, type 2KXXXXXXXXXXXXX
Charcot-Marie-Tooth disease, type 4A214400Graph: Charcot-Marie-Tooth disease, type 4AXXXXXXXXXXXXX
Charcot-Marie-Tooth disease, type 4B1601382Graph: Charcot-Marie-Tooth disease, type 4B1MouseHumanXXXXXXXXYeastXX
Charcot-Marie-Tooth disease, type 4B2604563Graph: Charcot-Marie-Tooth disease, type 4B2XXXXXXXXXXXXX
Charcot-Marie-Tooth disease, type 4D601455Graph: Charcot-Marie-Tooth disease, type 4DXHumanXXXXXXXXXXX
Charcot-Marie-Tooth neuropathy, X-linked dominant, 1302800Graph: Charcot-Marie-Tooth neuropathy, X-linked dominant, 1XHumanRatXXXXXXXXXX
Chediak-Higashi syndrome214500Graph: Chediak-Higashi syndromeXHumanXXXXXXXXXXX
Cherubism118400Graph: CherubismXHumanXXXXXXXXXXX
Chloride diarrhea, congenital, Finnish type214700Graph: Chloride diarrhea, congenital, Finnish typeMouseHumanRatXXXXXXXXXX
Cholestasis, benign recurrent intrahepatic243300Graph: Cholestasis, benign recurrent intrahepaticMouseHumanXXXXXXXXXXX
Cholestasis, familial intrahepatic, of pregnancy147480Graph: Cholestasis, familial intrahepatic, of pregnancyMouseHumanXWormXDictyXXXXYeastXPfalc
Cholestasis, progressive familial intrahepatic 1211600Graph: Cholestasis, progressive familial intrahepatic 1MouseHumanXXXXXXXXXXX
Cholestasis, progressive familial intrahepatic 2601847Graph: Cholestasis, progressive familial intrahepatic 2MouseHumanRatWormXDictyXXXXYeastXPfalc
Cholestasis, progressive familial intrahepatic 3602347Graph: Cholestasis, progressive familial intrahepatic 3MouseHumanXWormXDictyXXXXYeastXPfalc
Cholestasis, progressive familial intrahepatic 4607765Graph: Cholestasis, progressive familial intrahepatic 4XHumanRatXXXXXXXXXX
Chondrocalcinosis 2118600Graph: Chondrocalcinosis 2MouseHumanXXXXXXXXXXX
Chondrodysplasia punctata, X-linked dominant302960Graph: Chondrodysplasia punctata, X-linked dominantMouseHumanRatXXXXXXXXXX
Chondrodysplasia punctata, X-linked recessive302950Graph: Chondrodysplasia punctata, X-linked recessiveXHumanXXXXXXXXXXX
Chondrodysplasia punctata, rhizomelic, type 2222765Graph: Chondrodysplasia punctata, rhizomelic, type 2MouseHumanRatXXXXXXXXXX
Chondrodysplasia, Grebe type200700Graph: Chondrodysplasia, Grebe typeMouseHumanXXXXXXXXXXX
Chondrosarcoma215300Graph: ChondrosarcomaMouseHumanXXXXXXXXXXX
Chorea, hereditary benign118700Graph: Chorea, hereditary benignMouseXRatWormXXXXXXXXX
Choreoacanthocytosis200150Graph: ChoreoacanthocytosisXXXXXXXXXXYeastXX
Choroideremia303100Graph: ChoroideremiaMouseHumanRatXXXXXXXXXX
Chromosome 22q13.3 deletion syndrome606232Graph: Chromosome 22q13.3 deletion syndromeXXXXXXXXXXXXX
Chronic granulomatous disease due to deficiency of NCF-1233700Graph: Chronic granulomatous disease due to deficiency of NCF-1MouseHumanXXXXXXXXXXX
Chronic granulomatous disease, X-linked306400Graph: Chronic granulomatous disease, X-linkedXHumanRatXXDictyXXXXYeastXX
Chronic granulomatous disease, autosomal, due to deficiency of CYBA233690Graph: Chronic granulomatous disease, autosomal, due to deficiency of CYBAXHumanRatXXXXXXXXXX
Chudley-Lowry syndrome309490Graph: Chudley-Lowry syndromeMouseHumanRatWormXXXXXXXXX
Chylomicron retention disease246700Graph: Chylomicron retention diseaseXXXXXXXXXXYeastXX
Chylomicron retention disease with Marinesco-Sjogren syndrome607692Graph: Chylomicron retention disease with Marinesco-Sjogren syndromeXXXXXXXXXXYeastXX
Ciliary dyskinesia, primary, 1242650Graph: Ciliary dyskinesia, primary, 1XHumanXXXXXXXXXXX
Cirrhosis, North American Indian childhood type604901Graph: Cirrhosis, North American Indian childhood typeXXXXXXXXXXYeastXX
Citrullinemia215700Graph: CitrullinemiaMouseHumanRatXXXXXXXYeastXX
Citrullinemia, adult-onset type II603471Graph: Citrullinemia, adult-onset type IIMouseHumanXXXXXXXXYeastXX
Citrullinemia, type II, neonatal-onset605814Graph: Citrullinemia, type II, neonatal-onsetMouseHumanXXXXXXXXYeastXX
Cleft lip/palate ectodermal dysplasia syndrome225000Graph: Cleft lip/palate ectodermal dysplasia syndromeMouseHumanXXXXXXXXXXX
Cleft lip/palate, nonsyndromic608874Graph: Cleft lip/palate, nonsyndromicMouseHumanXWormXXXXXXXXX
Cleft palate with ankyloglossia303400Graph: Cleft palate with ankyloglossiaXHumanXXXXXXXXXXX
Cleidocranial dysplasia119600Graph: Cleidocranial dysplasiaMouseHumanXXXXXXXXXXX
Coenzyme Q10 deficiency607426Graph: Coenzyme Q10 deficiencyMouseHumanXXXXXXXXYeastXX
Coffin-Lowry syndrome303600Graph: Coffin-Lowry syndromeMouseHumanXXXXXXXXXXX
Cohen syndrome216550Graph: Cohen syndromeXXXXXXXXXXXXX
Cold-induced autoinflammatory syndrome, familial120100Graph: Cold-induced autoinflammatory syndrome, familialXHumanXXXDictyXXXXXXX
Cold-induced sweating syndrome272430Graph: Cold-induced sweating syndromeXHumanXXXXXXXXXXX
Coloboma, ocular120200Graph: Coloboma, ocularMouseHumanRatWormXXChickenXXXYeastXX
Colon cancer, somatic114500Graph: Colon cancer, somaticMouseHumanRatWormXDictyXXXXYeastPombeX
Colorectal adenomatous polyposis, autosomal recessive, with pilomatricomas132600Graph: Colorectal adenomatous polyposis, autosomal recessive, with pilomatricomasMouseHumanRatWormXXXZfinXXXXX
Colorectal cancer114500Graph: Colorectal cancerMouseHumanRatWormXDictyXXXXYeastPombeX
Colorectal cancer, hereditary nonpolyposis, type 2609310Graph: Colorectal cancer, hereditary nonpolyposis, type 2MouseHumanXXXXXXXXYeastXX
Colorectal cancer, somatic114500Graph: Colorectal cancer, somaticMouseHumanRatWormXDictyXXXXYeastPombeX
Combined factor V and VIII deficiency227300Graph: Combined factor V and VIII deficiencyMouseHumanXXXXXXXXXXX
Combined immunodeficiency, X-linked, moderate312863Graph: Combined immunodeficiency, X-linked, moderateMouseHumanRatXXXXXXXXXX
Complex V, mitochondrial respiratory chain, deficiency of604273Graph: Complex V, mitochondrial respiratory chain, deficiency ofXXXXXXXXXXYeastXX
Cone dystrophy-1304020Graph: Cone dystrophy-1MouseHumanXXXXXXXXXXX
Cone dystrophy-3602093Graph: Cone dystrophy-3MouseHumanXXXXXXXXXXX
Cone-rod dystrophy300029Graph: Cone-rod dystrophyMouseHumanXXXXXXXXXXX
Cone-rod dystrophy 3604116Graph: Cone-rod dystrophy 3MouseHumanXXXXXXXXXXX
Cone-rod dystrophy 9608194Graph: Cone-rod dystrophy 9MouseXXXXXXXXXXXX
Cone-rod retinal dystrophy-2120970Graph: Cone-rod retinal dystrophy-2MouseHumanXXXXXXXXXXX
Congenital bilateral absence of vas deferens277180Graph: Congenital bilateral absence of vas deferensXHumanRatXXXXXXXXXX
Congenital disorder of glycosylation, type IIc266265Graph: Congenital disorder of glycosylation, type IIcXXXXXXXXXXXXX
Congenital disorder of glycosylation, type IId607091Graph: Congenital disorder of glycosylation, type IIdMouseXXXXXXXXXXXX
Congenital disorder of glycosylation, type IIe608779Graph: Congenital disorder of glycosylation, type IIeXHumanXXXXXXXXXXX
Congenital disorder of glycosylation, type Ic603147Graph: Congenital disorder of glycosylation, type IcXHumanXXXXXXXXYeastXX
Congenital disorder of glycosylation, type Id601110Graph: Congenital disorder of glycosylation, type IdXXXXXXXXXXXXX
Congenital disorder of glycosylation, type Ie608799Graph: Congenital disorder of glycosylation, type IeMouseHumanXXXXXXXXYeastXX
Congenital disorder of glycosylation, type Ig