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) - - 1005 979 ADARB1, AP1G1, DDB1, DHX30, EIF2C1, EIF2C2, GLTSCR1, IQSEC1, MAPK1, MAPK8IP3, NCDN, NCKAP1, NTNG2, POLR2A, POU3F3, PPM1D, SATB1, SCAF4, SHMT2, TAOK1, TET3, VPS4A - -
05920 NEDMIAL neurodevelopmental disorder with severe motor impairment and absent language (NEDMIAL) 617804 AD 0 0 DHX30 - -
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