MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Dehydrated hereditary stomatocytosis

ORPHA:3202Kr.
Autosomal dominant

Dejerine-Sottas syndrome

ORPHA:64748Kr.
Autosomal dominant, Autosomal recessive, Not applicable

Delayed encephalopathy due to carbon monoxide poisoning

ORPHA:306686Kr.

Delayed membranous cranial ossification

ORPHA:3034Malf.

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

ORPHA:3038Malf.

Deletion 5q35 syndrome

ORPHA:1627Malf.
Not applicable, Unknown

Delta-beta-thalassemia

ORPHA:231237Kr.
Autosomal recessive

Delta-sarcoglycan-related limb-girdle muscular dystrophy R6

ORPHA:219Kr.
Autosomal recessive

Dementia pugilistica

ORPHA:97353Kr.

Dengue fever

ORPHA:99828Kr.
Not applicable

Dense deposit disease

ORPHA:93571His. subt.
Autosomal recessive

Dent disease

ORPHA:1652Kr.
X-linked recessive

Dent disease type 1

ORPHA:93622Kl. subt.
X-linked recessive

Dent disease type 2

ORPHA:93623Kl. subt.
X-linked recessive

Dental ankylosis

ORPHA:1077Malf.

Dentatorubral pallidoluysian atrophy

ORPHA:101Kr.
Autosomal dominant

Dentin dysplasia

ORPHA:1653Kr.
Autosomal dominant

Dentin dysplasia type I

ORPHA:99789Kl. subt.
Autosomal dominant, Autosomal recessive

Dentin dysplasia type II

ORPHA:99791Kl. subt.
Autosomal dominant

Dentin dysplasia-sclerotic bones syndrome

ORPHA:99792Kr.

Dentinogenesis imperfecta

ORPHA:49042Kr.
Autosomal dominant

Dentinogenesis imperfecta type 2

ORPHA:166260Kl. subt.
Autosomal dominant

Dentinogenesis imperfecta type 3

ORPHA:166265Kl. subt.
Autosomal dominant

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

ORPHA:71267Malf.
Autosomal recessive