All diseases

10 entries on 1 page. Showing entries 1 - 10.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02894 - Polymicrogyria, asymmetric 610031 - - - TUBB2B - -
03260 - macrothrombocytopenia, autosomal dominant, TUBB1-related 613112 - - - TUBB1 - -
03527 CDCBM-1 dysplasia ,cortical, complex, with other brain malformations (CDCBM-1) 614039 - - - TUBB3 - -
04077 CDCBM-5 dysplasia ,cortical, complex, with other brain malformations, type 5 (CDCBM-5) 615763 - - - TUBB2A - -
04081 CDCBM-6 dysplasia ,cortical, complex, with other brain malformations, type 6 (CDCBM-6) 615771 - - - TUBB - -
05050 CFEOM-3A fibrosis of extraocular muscles, congenital, type 3A (CFEOM-3A) 600638 - - - TUBB3 - -
00793 CPI cleft palate, isolated (CPI) 119540 - - - SATB2, UBB - -
05051 DYT-4 dystonia, type 4, torsion, autosomal dominant (DYT-4) 128101 - - - TUBB4A - -
05052 HLD-6 leukodystrophy, hypomyelinating, type 6 (HLD-6) 612438 - - - TUBB4A - -
00139 ID intellectual disability (ID) - - - - AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 515 more - -
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