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

Denys-Drash syndrome

ORPHA:220Kr.
Autosomal dominant

Dermatitis herpetiformis

ORPHA:1656Kr.
Not applicable

Dermatofibrosarcoma protuberans

ORPHA:31112Kr.
Not applicable

Dermatoleukodystrophy

ORPHA:1659Kr.
Autosomal recessive

Dermatomyositis

ORPHA:221Kr.
Not applicable

Dermatopathia pigmentosa reticularis

ORPHA:86920Kr.
Autosomal dominant

Dermatosparaxis Ehlers-Danlos syndrome

ORPHA:1901Kr.
Autosomal recessive

Dermochondrocorneal dystrophy

ORPHA:79149Kr.
Autosomal recessive

Desmin-related myopathy with Mallory body-like inclusions

ORPHA:84132Kr.
Autosomal recessive

Desminopathy

ORPHA:98909Kr.
Autosomal dominant, Autosomal recessive

Desmoid tumor

ORPHA:873Kr.
Not applicable, Unknown

Desmoplastic infantile astrocytoma/ganglioglioma

ORPHA:251940Kr.
Not applicable

Desmoplastic small round cell tumor

ORPHA:83469Kr.
Not applicable

Desmosterolosis

ORPHA:35107Kr.
Autosomal recessive

Developmental and epileptic encephalopathy with spike-wave activation in sleep

ORPHA:725Kr.
Autosomal dominant, Not applicable

Developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency

ORPHA:289307Kr.
Autosomal recessive

Developmental delay with autism spectrum disorder and gait instability

ORPHA:329195Kr.
Autosomal recessive

Developmental delay-immunodeficiency-leukoencephalopathy-hypohomocysteinemia syndrome

ORPHA:619979Kr.
Autosomal dominant

Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome

ORPHA:660017Kr.
Autosomal dominant

Diamond-Blackfan anemia

ORPHA:124Kr.
Autosomal dominant

Dianzani autoimmune lymphoproliferative disease

ORPHA:275523Kr.
Unknown

Diaphyseal medullary stenosis-bone malignancy syndrome

ORPHA:85182Kr.
Autosomal dominant

Diastrophic dysplasia

ORPHA:628Kr.
Autosomal recessive

Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency

ORPHA:276603Kr.
Autosomal recessive