MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

Nipah virus disease

ORPHA:99825Disease

Nocardiosis

ORPHA:31204Disease
Not applicable

Nodal marginal zone B-cell lymphoma

ORPHA:86867Disease
Not applicable

Nodular fasciitis

ORPHA:477742Disease
Not applicable

Nodular lymphocyte predominant Hodgkin lymphoma

ORPHA:86893Disease
Unknown

Nodular neuronal heterotopia

ORPHA:2149Morph.
Autosomal dominant, Autosomal recessive, X-linked dominant

Nodular non-suppurative panniculitis

ORPHA:33577Disease
Not applicable

Nodular regenerative hyperplasia of the liver

ORPHA:48372Hist. sub.
Not applicable

Nodular urticaria pigmentosa

ORPHA:158772Clin. sub.
Autosomal dominant, Unknown

Noma

ORPHA:2700Disease

Non-24-hour sleep-wake syndrome

ORPHA:73267Disease
Unknown

Non-Hodgkin lymphoma

ORPHA:547Cat.

Non-acquired combined pituitary hormone deficiency

ORPHA:467Cat.

Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome

ORPHA:231720Malform.
Autosomal recessive

Non-acquired isolated growth hormone deficiency

ORPHA:631Disease
Autosomal dominant, Autosomal recessive, X-linked recessive

Non-acquired panhypopituitarism

ORPHA:90695Disease
Autosomal recessive, X-linked recessive

Non-amyloid fibrillary glomerulopathy

ORPHA:97566Disease
Not applicable

Non-amyloid monoclonal immunoglobulin deposition disease

ORPHA:86861Disease

Non-classic congenital lipoid adrenal hyperplasia due to STAR deficency

ORPHA:325529Clin. sub.
Autosomal recessive

Non-distal deletion 10q syndrome

ORPHA:1581Malform.

Non-distal deletion 12q syndrome

ORPHA:96160Malform.

Non-distal duplication 10q syndrome

ORPHA:1695Malform.

Non-distal duplication 13q syndrome

ORPHA:1702Malform.

Non-distal duplication 9q syndrome

ORPHA:96112Malform.