MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Nipah virus disease

ORPHA:99825Kr.

Nocardiosis

ORPHA:31204Kr.
Not applicable

Nodal marginal zone B-cell lymphoma

ORPHA:86867Kr.
Not applicable

Nodular fasciitis

ORPHA:477742Kr.
Not applicable

Nodular lymphocyte predominant Hodgkin lymphoma

ORPHA:86893Kr.
Unknown

Nodular neuronal heterotopia

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

Nodular non-suppurative panniculitis

ORPHA:33577Kr.
Not applicable

Nodular regenerative hyperplasia of the liver

ORPHA:48372His. subt.
Not applicable

Nodular urticaria pigmentosa

ORPHA:158772Kl. subt.
Autosomal dominant, Unknown

Noma

ORPHA:2700Kr.

Non-24-hour sleep-wake syndrome

ORPHA:73267Kr.
Unknown

Non-Hodgkin lymphoma

ORPHA:547Kat.

Non-acquired combined pituitary hormone deficiency

ORPHA:467Kat.

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

ORPHA:231720Malf.
Autosomal recessive

Non-acquired isolated growth hormone deficiency

ORPHA:631Kr.
Autosomal dominant, Autosomal recessive, X-linked recessive

Non-acquired panhypopituitarism

ORPHA:90695Kr.
Autosomal recessive, X-linked recessive

Non-amyloid fibrillary glomerulopathy

ORPHA:97566Kr.
Not applicable

Non-amyloid monoclonal immunoglobulin deposition disease

ORPHA:86861Kr.

Non-classic congenital lipoid adrenal hyperplasia due to STAR deficency

ORPHA:325529Kl. subt.
Autosomal recessive

Non-distal deletion 10q syndrome

ORPHA:1581Malf.

Non-distal deletion 12q syndrome

ORPHA:96160Malf.

Non-distal duplication 10q syndrome

ORPHA:1695Malf.

Non-distal duplication 13q syndrome

ORPHA:1702Malf.

Non-distal duplication 9q syndrome

ORPHA:96112Malf.