MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Didymosis aplasticosebacea

ORPHA:370046Kr.
Not applicable

Diencephalic syndrome

ORPHA:1672Kr.
Not applicable

Diencephalic-mesencephalic junction dysplasia

ORPHA:319192Morph.
Autosomal recessive

Dietary iron overload disease

ORPHA:139507Kr.
Not applicable

Diethylstilbestrol syndrome

ORPHA:1916Malf.
Not applicable

Difference of sex development-intellectual disability syndrome

ORPHA:2983Kr.
Unknown

Differentiated thyroid carcinoma

ORPHA:146Kr.
Not applicable

Diffuse alveolar hemorrhage

ORPHA:90060Clinical syndrome
Not applicable

Diffuse astrocytoma

ORPHA:251595Kr.

Diffuse capillary malformation with overgrowth

ORPHA:714737Morph.
Not applicable

Diffuse cerebral and cerebellar atrophy-intractable seizures-progressive microcephaly syndrome

ORPHA:404437Malf.
Autosomal recessive

Diffuse cutaneous mastocytosis

ORPHA:79456Kr.
Not applicable

Diffuse cutaneous systemic sclerosis

ORPHA:220393Kl. subt.
Multigenic/multifactorial, Not applicable

Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia

ORPHA:617916Kr.

Diffuse intrinsic pontine glioma

ORPHA:497188Kr.

Diffuse large B-cell lymphoma

ORPHA:544Kl. gruppe
Multigenic/multifactorial, Not applicable

Diffuse large B-cell lymphoma of the central nervous system

ORPHA:300849Kr.
Multigenic/multifactorial, Not applicable

Diffuse lymphatic malformation

ORPHA:141209Malf.
Not applicable

Diffuse palmoplantar keratoderma with painful fissures

ORPHA:369999Kr.
Autosomal dominant

Diffuse palmoplantar keratoderma, Bothnian type

ORPHA:2337Kr.
Autosomal dominant

Diffuse palmoplantar keratoderma-acrocyanosis syndrome

ORPHA:86918Kr.
Autosomal dominant

Diffuse panbronchiolitis

ORPHA:171700Kr.
Multigenic/multifactorial

Digenic Alport syndrome

ORPHA:653722Kl. subt.
Autosomal dominant, Autosomal recessive

Digenic hemochromatosis

ORPHA:648581Kr.