Disease #06507 (OCNDS (Okur-Chung neurodevelopmental syndrome), OMIM:617062)

Official abbreviation OCNDS
Name Okur-Chung neurodevelopmental syndrome
OMIM ID 617062
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CSNK2A1
Associated tissues -
Disease features -
Remarks -

  Powered by LOVD v.3.0 Build 27
LOVD software ©2004-2022 Leiden University Medical Center 		There are currently no updates.