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"

16 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 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 precocious puberty

ORPHA:435554

Genetic precocious puberty in female

ORPHA:435564

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

Rare central precocious puberty

Gonadotropin-dependant precocious puberty · Rare CPP

ORPHA:650063

Rare central precocious puberty in female

Rare central precocious puberty in girl · Rare CPP in female

ORPHA:650070

Rare peripheral precocious puberty

ORPHA:178040

Rare peripheral precocious puberty in female

ORPHA:650187

Rare precocious puberty

ORPHA:95708

Rare precocious puberty in female

ORPHA:435561

Secondary central precocious puberty in female

Secondary central precocious puberty in girl · Secondary CPP in girl

ORPHA:650082

Secondary central precocious puberty in male

Secondary central precocious puberty in boy · Secondary CPP in male

ORPHA:650092