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 ×

Arginine vasopressin resistance

Nephrogenic diabetes insipidus

ORPHA:223

Arginine vasopressin resistance-intracranial calcification-short stature-facial dysmorphism syndrome

Nephrogenic diabetes insipidus-intracranial calcification-short stature-facial dysmorphism syndrome

ORPHA:3145

Acquired arginine vasopressin deficiency

Acquired CDI · Acquired neurogenic diabetes insipidus

ORPHA:95626

Arginine vasopressin deficiency

CDI · Neurogenic diabetes insipidus

ORPHA:178029

Hereditary arginine vasopressin deficiency

Hereditary CDI · Hereditary neurogenic diabetes insipidus

ORPHA:30925

Isolated permanent neonatal diabetes mellitus

Monogenic diabetes of infancy · Isolated PNDM

ORPHA:99885

Neonatal diabetes mellitus

NDM · Congenital diabetes mellitus

ORPHA:224

OBSOLETE: Congenital central diabetes insipidus

ORPHA:95501

OBSOLETE: Posttraumatic diabetes insipidus

ORPHA:95625