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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Dehydrated hereditary stomatocytosis

ORPHA:3202Disease
Autosomal dominant

Dejerine-Sottas syndrome

ORPHA:64748Disease
Autosomal dominant, Autosomal recessive, Not applicable

Delayed encephalopathy due to carbon monoxide poisoning

ORPHA:306686Disease

Delayed membranous cranial ossification

ORPHA:3034Malform.

Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome

ORPHA:3038Malform.

Deletion 5q35 syndrome

ORPHA:1627Malform.
Not applicable, Unknown

Delta-beta-thalassemia

ORPHA:231237Disease
Autosomal recessive

Delta-sarcoglycan-related limb-girdle muscular dystrophy R6

ORPHA:219Disease
Autosomal recessive

Dementia pugilistica

ORPHA:97353Disease

Dengue fever

ORPHA:99828Disease
Not applicable

Dense deposit disease

ORPHA:93571Hist. sub.
Autosomal recessive

Dent disease

ORPHA:1652Disease
X-linked recessive

Dent disease type 1

ORPHA:93622Clin. sub.
X-linked recessive

Dent disease type 2

ORPHA:93623Clin. sub.
X-linked recessive

Dental ankylosis

ORPHA:1077Malform.

Dentatorubral pallidoluysian atrophy

ORPHA:101Disease
Autosomal dominant

Dentin dysplasia

ORPHA:1653Disease
Autosomal dominant

Dentin dysplasia type I

ORPHA:99789Clin. sub.
Autosomal dominant, Autosomal recessive

Dentin dysplasia type II

ORPHA:99791Clin. sub.
Autosomal dominant

Dentin dysplasia-sclerotic bones syndrome

ORPHA:99792Disease

Dentinogenesis imperfecta

ORPHA:49042Disease
Autosomal dominant

Dentinogenesis imperfecta type 2

ORPHA:166260Clin. sub.
Autosomal dominant

Dentinogenesis imperfecta type 3

ORPHA:166265Clin. sub.
Autosomal dominant

Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome

ORPHA:71267Malform.
Autosomal recessive