Disease #01519 (CPPB1 (puberty, precocious, central, type 1 (CPPB1)), OMIM:176400)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CPPB1
Name	puberty, precocious, central, type 1 (CPPB1)
OMIM ID	176400
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KISS1R
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-10-19 16:09:55 +02:00 (CEST)

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