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 ×

Combined pituitary hormone deficiencies, genetic forms

Familial congenital hypopituitarism · Multiple pituitary hormone deficiencies, genetic forms

ORPHA:95494

Acquired pituitary hormone deficiency

ORPHA:95502

Non-acquired combined pituitary hormone deficiency

Congenital combined pituitary hormone deficiency · Congenital hypopituitarism

ORPHA:467

Non-acquired pituitary hormone deficiency

ORPHA:95488

OBSOLETE: Metastatic pituitary hormone deficiency

ORPHA:95504

Pituitary deficiency

ORPHA:101957

Pituitary hormone deficiency of meningeal origin

ORPHA:95505

Pituitary hormone deficiency of tumoral origin

ORPHA:95503

Pituitary hormone deficiency of vascular origin

ORPHA:95611