ORPHA:649929

Central precocious puberty in male

Synonyms: CPP in boy · CPP in male · Central precocious puberty in boy

Type: Clinical group
Group: Group of disorders
Status: active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

Names in Orphadata languages

10 of 12 languages

Lang	Name	Synonyms
en	Central precocious puberty in male	CPP in boy · CPP in male · Central precocious puberty in boy
fr	Puberté précoce centrale de l'homme	Puberté précoce centrale du garçon
de	Zentrale vorzeitige Pubertät bei Jungen	CPP beim Jungen · Pubertas praecox, zentrale, männliche Form · Zentral ausgelöste Pubertas praecox bei Jungen
es	Pubertad precoz central en el varón	PPC en el niño · PPC en el varón · Pubertad precoz central en el niño
it	Pubertà maschileprecoce centrale	CPP maschile · CPP nel ragazzo · Pubertà precoce centrale nel ragazzo
nl	Centrale pubertas praecox bij man	Centrale vroegtijdige puberteit bij man · CPP bij jongen · CPP bij man · Centrale pubertas praecox bij jongen
pt	Puberdade precoce central no indivíduo masculino	CPP no indivíduo masculino · CPP nos rapazes · Puberdade precoce central nos rapazes
pl	Przedwczesne dojrzewanie płciowe pochodzenia ośrodkowego u mężczyzny	= en
cs	Centrální předčasná puberta u chlapce	= en
uk	Центральне передчасне статеве дозрівання у хлопчиків	Центральне передчасне статеве дозрівання у хлопчика · CPP у хлопчика · CPP у чоловіків

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
UMLS	C5816736	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:97978Rare endocrine disease

Parents in the classifications (1):

ORPHA:650063Rare central precocious puberty
rare endocrine diseases

Children (2):

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/649929
This record as JSON: /data/d/649929.json