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Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер
Табылды 1,772 заболеваний (Мальф.) Қалпына келтіру

Emanuel syndrome

ORPHA:96170Мальф.

Emery-Nelson syndrome

ORPHA:1927Мальф.

Enamel-renal syndrome

ORPHA:1031Мальф.
Autosomal recessive

Endocrine-cerebro-osteodysplasia syndrome

ORPHA:199332Мальф.
Autosomal recessive

Endosteal hyperostosis, Worth type

ORPHA:2790Мальф.
Autosomal dominant

Endosteal sclerosis-cerebellar hypoplasia syndrome

ORPHA:85186Мальф.
Autosomal recessive

Eng-Strom syndrome

ORPHA:1937Мальф.
Autosomal dominant

Enlarged parietal foramina

ORPHA:60015Мальф.
Autosomal dominant

Epibulbar lipodermoid-preauricular appendage-polythelia syndrome

ORPHA:231742Мальф.
Autosomal dominant

Epidermolysis bullosa simplex with anodontia/hypodontia

ORPHA:2325Мальф.

Epilepsy-microcephaly-skeletal dysplasia syndrome

ORPHA:1948Мальф.
Autosomal recessive

Epiphyseal dysplasia-hearing loss-dysmorphism syndrome

ORPHA:1825Мальф.

Epiphyseal stippling-osteoclastic hyperplasia syndrome

ORPHA:1952Мальф.
Autosomal recessive

Ermine phenotype

ORPHA:999Мальф.
Autosomal recessive

Exostoses-anetodermia-brachydactyly type E syndrome

ORPHA:1962Мальф.
Unknown

Exstrophy-epispadias complex

ORPHA:322Мальф.
Multigenic/multifactorial

Extensor tendons of finger anomalies

ORPHA:3294Мальф.

External auditory canal atresia-vertical talus-hypertelorism syndrome

ORPHA:3023Мальф.
Autosomal dominant, Not applicable, Unknown

Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome

ORPHA:1964Мальф.
Autosomal dominant

Eyebrow duplication-syndactyly syndrome

ORPHA:3172Мальф.
Autosomal recessive

FATCO syndrome

ORPHA:2492Мальф.

FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome

ORPHA:404451Мальф.
Autosomal recessive

FOXP1 Syndrome

ORPHA:391372Мальф.
Autosomal dominant

Facial dysmorphism-Intellectual disability-rhombencephalosynapsis syndrome

ORPHA:693549Мальф.
Autosomal dominant