Disease #07059 (NEDCDS (neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects), OMIM:620083)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	NEDCDS
Name	neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects
OMIM ID	620083
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	HNRNPH1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-01-01 19:38:35 +01:00 (CET)
Date last edited	2024-01-01 19:41:26 +01:00 (CET)

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