MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Dehydrated hereditary stomatocytosis

ORPHA:3202Заболевание
Autosomal dominant

Dejerine-Sottas syndrome

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

Delayed encephalopathy due to carbon monoxide poisoning

ORPHA:306686Заболевание

Delayed membranous cranial ossification

ORPHA:3034Мальформация

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

ORPHA:3038Мальформация

Deletion 5q35 syndrome

ORPHA:1627Мальформация
Not applicable, Unknown

Delta-beta-thalassemia

ORPHA:231237Заболевание
Autosomal recessive

Delta-sarcoglycan-related limb-girdle muscular dystrophy R6

ORPHA:219Заболевание
Autosomal recessive

Dementia pugilistica

ORPHA:97353Заболевание

Dengue fever

ORPHA:99828Заболевание
Not applicable

Dense deposit disease

ORPHA:93571Гист. подтип
Autosomal recessive

Dent disease

ORPHA:1652Заболевание
X-linked recessive

Dent disease type 1

ORPHA:93622Клин. подтип
X-linked recessive

Dent disease type 2

ORPHA:93623Клин. подтип
X-linked recessive

Dental ankylosis

ORPHA:1077Мальформация

Dentatorubral pallidoluysian atrophy

ORPHA:101Заболевание
Autosomal dominant

Dentin dysplasia

ORPHA:1653Заболевание
Autosomal dominant

Dentin dysplasia type I

ORPHA:99789Клин. подтип
Autosomal dominant, Autosomal recessive

Dentin dysplasia type II

ORPHA:99791Клин. подтип
Autosomal dominant

Dentin dysplasia-sclerotic bones syndrome

ORPHA:99792Заболевание

Dentinogenesis imperfecta

ORPHA:49042Заболевание
Autosomal dominant

Dentinogenesis imperfecta type 2

ORPHA:166260Клин. подтип
Autosomal dominant

Dentinogenesis imperfecta type 3

ORPHA:166265Клин. подтип
Autosomal dominant

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

ORPHA:71267Мальформация
Autosomal recessive