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"

13 matching diseasesClear search ×

Secondary central precocious puberty in female

Secondary central precocious puberty in girl · Secondary CPP in girl

ORPHA:650082

Central precocious puberty in male

Central precocious puberty in boy · CPP in male

ORPHA:649929

Genetic central precocious puberty in female

Genetic central precocious puberty in girl · Genetic CPP in female

ORPHA:650077

Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance

Idiopathic SSNS with secondary steroid resistance · Secondary steroid-resistant nephrotic syndrome

ORPHA:567546

Primary central precocious puberty in male

Primary central precocious puberty in boy · Primary CPP in boy

ORPHA:650087

Pulmonary arterial hypertension associated with another disease

PAH · PAH associated with another disease

ORPHA:275791

Rare central precocious puberty in female

Rare central precocious puberty in girl · Rare CPP in female

ORPHA:650070

Secondary avascular necrosis

Secondary AVN

ORPHA:399169

Secondary central precocious puberty in male

Secondary central precocious puberty in boy · Secondary CPP in male

ORPHA:650092

Secondary hypereosinophilic syndrome

HES-R · Reactive hypereosinophilic syndrome

ORPHA:314962

Secondary polyarteritis nodosa

Secondary periarteritis nodosa · Secondary PAN

ORPHA:439746

Secondary pulmonary alveolar proteinosis

Secondary PAP

ORPHA:420259

Therapy related acute myeloid leukemia and myelodysplastic syndrome

Acute myeloid leukemia · AML

ORPHA:86846