Disease #05748 (HOD (hypopigmentation, organomegaly, and delayed myelination and development (HOD)), OMIM:618541)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	HOD
Name	hypopigmentation, organomegaly, and delayed myelination and development (HOD)
OMIM ID	618541
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CLCN7
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-05-18 09:30:05 +02:00 (CEST)
Date last edited	N/A

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