Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

9 matching diseasesClear search ×

Genetic central precocious puberty in male

Genetic central precocious puberty in boy · Genetic CPP in male

ORPHA:650097

Central precocious puberty in male

Central precocious puberty in boy · CPP in male

ORPHA:649929

Genetic bone tumor

ORPHA:183527

Genetic central precocious puberty

Genetic CPP

ORPHA:650182

Genetic central precocious puberty in female

Genetic central precocious puberty in girl · Genetic CPP in female

ORPHA:650077

Genetic interstitial lung disease

Genetic ILD

ORPHA:264992

Non-genetic central precocious puberty in male

Non-genetic central precocious puberty in boy · Non-genetic CPP in male

ORPHA:650102

Primary central precocious puberty in male

Primary central precocious puberty in boy · Primary CPP in boy

ORPHA:650087

Secondary central precocious puberty in male

Secondary central precocious puberty in boy · Secondary CPP in male

ORPHA:650092