Search Ontology:
Human Disease

central precocious puberty 2

Term ID
DOID:0112309
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. https://pubmed.ncbi.nlm.nih.gov/23738509/
References
Ontology
Human Disease   ( DOID:0112309 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models