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"

5 matching diseasesClear search ×

Acquired arginine vasopressin deficiency

Acquired CDI · Acquired neurogenic diabetes insipidus

ORPHA:95626

Acquired generalized lipodystrophy

Acquired lipoatrophic diabetes · Lawrence syndrome

ORPHA:79086

Arginine vasopressin deficiency

CDI · Neurogenic diabetes insipidus

ORPHA:178029

Arginine vasopressin resistance

Nephrogenic diabetes insipidus

ORPHA:223

Hereditary arginine vasopressin deficiency

Hereditary CDI · Hereditary neurogenic diabetes insipidus

ORPHA:30925