Search Ontology:
Human Disease
central precocious puberty 2
- Term ID
- DOID:0112309
- Synonyms
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- 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 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models