MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Distal hereditary motor neuropathy type 1

ORPHA:139518Заболевание
Autosomal dominant

Distal hereditary motor neuropathy type 2

ORPHA:139525Заболевание
Autosomal dominant

Distal hereditary motor neuropathy type 5

ORPHA:139536Заболевание
Autosomal dominant

Distal hereditary motor neuropathy type 7

ORPHA:139589Заболевание
Autosomal dominant

Distal hereditary motor neuropathy, Jerash type

ORPHA:139552Заболевание
Autosomal recessive

Distal limb deficiencies-micrognathia syndrome

ORPHA:1307Мальформация
Autosomal recessive

Distal monosomy 7q36 syndrome

ORPHA:1636Мальформация

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

ORPHA:700508Заболевание
Autosomal recessive

Distal myopathy

ORPHA:599Категория
Autosomal dominant, Autosomal recessive

Distal myopathy with anterior tibial onset

ORPHA:178400Заболевание
Autosomal recessive

Distal myopathy, Tateyama type

ORPHA:488650Заболевание
Autosomal dominant

Distal myopathy, Welander type

ORPHA:603Заболевание
Autosomal dominant

Distal myotilinopathy

ORPHA:98911Заболевание
Autosomal dominant

Distal renal tubular acidosis

ORPHA:18Заболевание
Autosomal dominant, Autosomal recessive, Not applicable

Distal renal tubular acidosis with anemia

ORPHA:93610Клин. подтип
Autosomal dominant

Distal spinal muscular atrophy type 3

ORPHA:139547Заболевание
Autosomal recessive

Distal triplication 15q syndrome

ORPHA:314588Этиол. подтип
Not applicable, Unknown

Distomatosis

ORPHA:1685Клин. группа
Not applicable

Dobrow syndrome

ORPHA:3262Мальформация

Dominant hypophosphatemia with nephrolithiasis or osteoporosis

ORPHA:244305Заболевание
Autosomal dominant

Donnai-Barrow syndrome

ORPHA:2143Мальформация
Autosomal recessive

Donohue syndrome

ORPHA:508Мальформация
Autosomal recessive

Dopa-responsive dystonia

ORPHA:255Клин. группа
Autosomal dominant, Autosomal recessive, Not applicable

Dopa-responsive dystonia due to sepiapterin reductase deficiency

ORPHA:70594Заболевание
Autosomal recessive