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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Ebola hemorrhagic fever

ORPHA:319218Ауру
Not applicable

Ebstein malformation of the tricuspid valve

ORPHA:1880Морф.
Autosomal dominant, Not applicable

Ectodermal dysplasia syndrome

ORPHA:79373Сан.

Ectodermal dysplasia with agenesis of maxillary lateral incisors and mandibular anterior teeth

ORPHA:708036Мальф.
Autosomal recessive

Ectodermal dysplasia with natal teeth, Turnpenny type

ORPHA:69083Мальф.
Autosomal dominant

Ectodermal dysplasia with oligodontia-hand and foot malformation-hypoplastic nipples

ORPHA:708043Мальф.
Autosomal dominant

Ectodermal dysplasia, trichoodontoonychial type

ORPHA:1818Мальф.

Ectodermal dysplasia-blindness syndrome

ORPHA:1806Мальф.
Autosomal recessive

Ectodermal dysplasia-hyperhidrosis-cutaneous syndactyly syndrome

ORPHA:247827Мальф.
Autosomal recessive

Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome

ORPHA:1812Мальф.
X-linked recessive

Ectodermal dysplasia-natal teeth-skin abscesses-plantar hyperkeratosis-hearing impairment

ORPHA:708014Мальф.

Ectodermal dysplasia-pili torti-cutaneous syndactyly syndrome

ORPHA:247820Мальф.
Autosomal recessive

Ectodermal dysplasia-sensorineural deafness syndrome

ORPHA:1883Мальф.
Autosomal recessive

Ectodermal dysplasia-skin fragility syndrome

ORPHA:158668Ауру
Autosomal recessive

Ectopia cordis

ORPHA:448270Морф.
Not applicable

Ectopia lentis-chorioretinal dystrophy-myopia syndrome

ORPHA:1884Ауру
Autosomal recessive

Ectopic aldosterone-producing tumor

ORPHA:231632Ауру
Not applicable

Ectrodactyly-polydactyly syndrome

ORPHA:1892Мальф.

Edinburgh malformation syndrome

ORPHA:1895Мальф.
Unknown

Ehlers-Danlos syndrome

ORPHA:98249Клин. топ
Autosomal dominant, Autosomal recessive, X-linked recessive

Ehlers-Danlos/osteogenesis imperfecta syndrome

ORPHA:230857Ауру
Autosomal dominant

Ehrlichiosis

ORPHA:1902Ауру

Eiken syndrome

ORPHA:79106Мальф.
Autosomal recessive

Eisenmenger syndrome

ORPHA:97214Мальф.
Not applicable