Term Name: central precocious puberty 2
Synonyms: CPPB2
Definition: A central precocious puberty that has_material_basis_in heterozygous mutation on the paternal allele of the MKRN3 gene on chromosome 15q11.2.
Ontology: Human Disease [DOID:0112309]   ( DOID:0112309 )

Relationships
is a type of: autosomal dominant disease central precocious puberty