FB2026_02 , released June 18, 2026
FB2026_02 , released June 18, 2026
CV Term Report
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General Information
Term central precocious puberty 2 ID (Ontology) DOID:0112309 (Human Disease)
Definition A central precocious puberty that has_material_basis_in heterozygous mutation on the paternal allele of the MKRN3 gene on chromosome 15q11.2.
Also Known As "CPPB2"
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 Genes
 central precocious puberty 2
 for disease ribbon | central precocious puberty 2
 model of | central precocious puberty 2
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autosomal genetic disease
 |__autosomal dominant disease__
endocrine system disease        |
 |__central precocious puberty__|
                                central precocious puberty 2  3 rec.
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Is a autosomal dominant disease
central precocious puberty
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Synonyms
  • "CPPB2" EXACT OMO:0003012
Secondary IDs
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MIM:615346