MEDLIB
Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Dehydrated hereditary stomatocytosis

ORPHA:3202Ауру
Autosomal dominant

Dejerine-Sottas syndrome

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

Delayed encephalopathy due to carbon monoxide poisoning

ORPHA:306686Ауру

Delayed membranous cranial ossification

ORPHA:3034Мальф.

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

ORPHA:3038Мальф.

Deletion 5q35 syndrome

ORPHA:1627Мальф.
Not applicable, Unknown

Delta-beta-thalassemia

ORPHA:231237Ауру
Autosomal recessive

Delta-sarcoglycan-related limb-girdle muscular dystrophy R6

ORPHA:219Ауру
Autosomal recessive

Dementia pugilistica

ORPHA:97353Ауру

Dengue fever

ORPHA:99828Ауру
Not applicable

Dense deposit disease

ORPHA:93571Гист. под.
Autosomal recessive

Dent disease

ORPHA:1652Ауру
X-linked recessive

Dent disease type 1

ORPHA:93622Клин. под.
X-linked recessive

Dent disease type 2

ORPHA:93623Клин. под.
X-linked recessive

Dental ankylosis

ORPHA:1077Мальф.

Dentatorubral pallidoluysian atrophy

ORPHA:101Ауру
Autosomal dominant

Dentin dysplasia

ORPHA:1653Ауру
Autosomal dominant

Dentin dysplasia type I

ORPHA:99789Клин. под.
Autosomal dominant, Autosomal recessive

Dentin dysplasia type II

ORPHA:99791Клин. под.
Autosomal dominant

Dentin dysplasia-sclerotic bones syndrome

ORPHA:99792Ауру

Dentinogenesis imperfecta

ORPHA:49042Ауру
Autosomal dominant

Dentinogenesis imperfecta type 2

ORPHA:166260Клин. под.
Autosomal dominant

Dentinogenesis imperfecta type 3

ORPHA:166265Клин. под.
Autosomal dominant

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

ORPHA:71267Мальф.
Autosomal recessive