MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Distal hereditary motor neuropathy type 1

ORPHA:139518Kr.
Autosomal dominant

Distal hereditary motor neuropathy type 2

ORPHA:139525Kr.
Autosomal dominant

Distal hereditary motor neuropathy type 5

ORPHA:139536Kr.
Autosomal dominant

Distal hereditary motor neuropathy type 7

ORPHA:139589Kr.
Autosomal dominant

Distal hereditary motor neuropathy, Jerash type

ORPHA:139552Kr.
Autosomal recessive

Distal limb deficiencies-micrognathia syndrome

ORPHA:1307Malf.
Autosomal recessive

Distal monosomy 7q36 syndrome

ORPHA:1636Malf.

Distal muscle weakness-foot deformity-elevated sorbitol level-hereditary motor neuropathy

ORPHA:700508Kr.
Autosomal recessive

Distal myopathy

ORPHA:599Kat.
Autosomal dominant, Autosomal recessive

Distal myopathy with anterior tibial onset

ORPHA:178400Kr.
Autosomal recessive

Distal myopathy, Tateyama type

ORPHA:488650Kr.
Autosomal dominant

Distal myopathy, Welander type

ORPHA:603Kr.
Autosomal dominant

Distal myotilinopathy

ORPHA:98911Kr.
Autosomal dominant

Distal renal tubular acidosis

ORPHA:18Kr.
Autosomal dominant, Autosomal recessive, Not applicable

Distal renal tubular acidosis with anemia

ORPHA:93610Kl. subt.
Autosomal dominant

Distal spinal muscular atrophy type 3

ORPHA:139547Kr.
Autosomal recessive

Distal triplication 15q syndrome

ORPHA:314588Ätl. subt.
Not applicable, Unknown

Distomatosis

ORPHA:1685Kl. gruppe
Not applicable

Dobrow syndrome

ORPHA:3262Malf.

Dominant hypophosphatemia with nephrolithiasis or osteoporosis

ORPHA:244305Kr.
Autosomal dominant

Donnai-Barrow syndrome

ORPHA:2143Malf.
Autosomal recessive

Donohue syndrome

ORPHA:508Malf.
Autosomal recessive

Dopa-responsive dystonia

ORPHA:255Kl. gruppe
Autosomal dominant, Autosomal recessive, Not applicable

Dopa-responsive dystonia due to sepiapterin reductase deficiency

ORPHA:70594Kr.
Autosomal recessive