Disease #07180 (IFAP2 (ichthyosis, follicular, with atrichia and photophobia syndrome, type 2), OMIM:619016)

Global Variome shared LOVD

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Official abbreviation	IFAP2
Name	ichthyosis, follicular, with atrichia and photophobia syndrome, type 2
OMIM ID	619016
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SREBF1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2025-09-22 12:51:00 +02:00 (CEST)
Date last edited	N/A

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