All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05111 HMN neuropathy, motor, distal, hereditary (HMN) - - 109 106 GBF1, WARS - -
06237 HMN9 Neuronopathy, distal hereditary motor, type IX 617721 AD - - WARS - -
00139 ID intellectual disability (ID) - - 2695 2377 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 553 more - -
05894 NEMMLAS neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with/without seizures (NEMMLAS) 617710 AR - - WARS2 - -
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