Disease #03507 (CPHD6 (hormone deficiency, pituitary, combined, type 6), OMIM:613986)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CPHD6
Name	hormone deficiency, pituitary, combined, type 6
OMIM ID	613986
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	OTX2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2023-12-23 15:03:30 +01:00 (CET)

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