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Metadata
ID	DOID:0112309
Name	central precocious puberty 2
Definition	A central precocious puberty that has_material_basis_in heterozygous mutation on the paternal allele of the MKRN3 gene on chromosome 15q11.2. https://pubmed.ncbi.nlm.nih.gov/23738509/
Xrefs	MIM:615346
Synonyms	CPPB2 [EXACT]
Parent Relationships	is_a autosomal dominant disease is_a central precocious puberty
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance