Disease #05577 (DEDSSH (developmental delay with short stature, dysmorphic features, and sparse hair (DEDSSH)), OMIM:616901)

Official abbreviation	DEDSSH
Name	developmental delay with short stature, dysmorphic features, and sparse hair (DEDSSH)
OMIM ID	616901
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	1
Associated with 1 gene	DPH1
Associated tissues	-
Disease features	autosomal recessive
Remarks	-
Date created	2019-02-22 15:50:29 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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