Disease #01535 (PTOS1 (ptosis, hereditary congenital, type 1 (PTOS1)), OMIM:178300)

Global Variome shared LOVD

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Official abbreviation	PTOS1
Name	ptosis, hereditary congenital, type 1 (PTOS1)
OMIM ID	178300
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	1
Associated with 1 gene	ZFHX4
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-05-10 11:22:57 +02:00 (CEST)

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