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DO Term : central precocious puberty 2 [DOID:0112309] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A central precocious puberty that has_material_basis_in heterozygous mutation on the paternal allele of the MKRN3 gene on chromosome 15q11.2.

synonyms:
CPPB2,
OMIM:615346,
615346

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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