MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

Nodular lymphocyte predominant Hodgkin lymphoma

ORPHA:86893Kr.
Unknown

Nodular non-suppurative panniculitis

ORPHA:33577Kr.
Not applicable

Noma

ORPHA:2700Kr.

Non-24-hour sleep-wake syndrome

ORPHA:73267Kr.
Unknown

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-functioning neuroendocrine tumor of pancreas

ORPHA:506075Kr.

Non-functioning paraganglioma

ORPHA:94080Kr.

Non-functioning pituitary adenoma

ORPHA:91349Kr.
Not applicable

Non-hypoproteinemic hypertrophic gastropathy

ORPHA:329883Kr.
Autosomal dominant

Non-insulinoma pancreatogenous hypoglycemia syndrome

ORPHA:276608Kr.
Autosomal dominant, Not applicable

Non-involuting congenital hemangioma

ORPHA:141179Kr.
Not applicable

Non-progressive cerebellar ataxia with intellectual disability

ORPHA:314647Kr.
Autosomal dominant

Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy

ORPHA:436271Kr.
Autosomal recessive

Non-recovering obstetric brachial plexus lesion

ORPHA:439202Kr.
Not applicable

Non-seminomatous germ cell tumor of testis

ORPHA:363494Kr.
Not applicable

Non-specific autoimmune brainstem encephalitis with characteristic antibodies

ORPHA:624199Kr.

Non-specific autoimmune brainstem encephalitis without characteristic antibodies

ORPHA:624216Kr.

Non-specific autoimmune cerebellar ataxia without characteristic antibodies

ORPHA:624268Kr.

Non-specific autoimmune supratentorial encephalitis with characteristic antibodies

ORPHA:624166Kr.

Non-specific autoimmune supratentorial encephalitis without characteristic antibodies

ORPHA:624178Kr.

Non-specific early-onset epileptic encephalopathy

ORPHA:442835Kr.
Autosomal dominant, Autosomal recessive, Not applicable, X-linked recessive