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
06116 NEDHELS;DYSEIDD neurodevelopmental disorder with hypotonia, impaired expressive language, and with or without seizures (DYSEIDD) 617171 AR - - DEAF1 - -
04442 VSVS;MRD24 Vulto-van Silfout-de Vries syndrome (MRD-24) 615828 AD 1 1 DEAF1 - -
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