OBO ID: DOID:0112309
Term Name: central precocious puberty 2 Search Ontology:
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 central precocious puberty 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MKRN3 Precocious puberty, central, 2
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.