All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05611 NDD neurodevelopmental delay (NDD) - - 1412 1383 ADARB1, AP1G1, ATP9A, DDB1, DHX30, EIF2C1, EIF2C2, GLTSCR1, GRIA2, HIST1H4C, HIST1H4D, HIST1H4E, HIST1H4F, HIST1H4I, HIST1H4J, IQSEC1, MAN2C1, MAPK1, MAPK8IP3, NCDN, 19 more - -
05920 NEDMIAL neurodevelopmental disorder with severe motor impairment and absent language (NEDMIAL) 617804 AD 0 0 DHX30 - -
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