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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

Crouzon syndrome-acanthosis nigricans syndrome

ORPHA:93262Мальф.
Autosomal dominant, Not applicable

Cryptomicrotia-brachydactyly-excess fingertip arch syndrome

ORPHA:1547Мальф.
Autosomal dominant

Cryptorchidism-arachnodactyly-intellectual disability syndrome

ORPHA:1548Мальф.

Currarino syndrome

ORPHA:1552Мальф.
Autosomal dominant, Not applicable

Curry-Jones syndrome

ORPHA:1553Мальф.
Not applicable

Cutaneous mastocytosis-deafness-microtia syndrome

ORPHA:2135Мальф.
Autosomal recessive

Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome

ORPHA:1555Мальф.
Autosomal dominant

Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies

ORPHA:221145Мальф.
Autosomal recessive

Cutis laxa-Marfanoid syndrome

ORPHA:171719Мальф.

Cutis marmorata telangiectatica congenita

ORPHA:1556Мальф.
Not applicable

Cyprus facial-neuromusculoskeletal syndrome

ORPHA:2674Мальф.
Autosomal dominant

Czeizel-Losonci syndrome

ORPHA:2437Мальф.
Autosomal dominant

DNMT3A-related microcephalic dwarfism

ORPHA:658595Мальф.
Autosomal dominant

DONSON-related microcephaly-short stature-limb abnormalities spectrum

ORPHA:572761Мальф.
Autosomal recessive

DOORS syndrome

ORPHA:79500Мальф.
Autosomal recessive

DYRK1A-related intellectual disability syndrome

ORPHA:464306Мальф.
Autosomal dominant, Not applicable, Unknown

Dahlberg-Borer-Newcomer syndrome

ORPHA:1563Мальф.
Autosomal recessive, X-linked recessive

Dandy-Walker malformation-postaxial polydactyly syndrome

ORPHA:1566Мальф.
Autosomal recessive

Deaf blind hypopigmentation syndrome, Yemenite type

ORPHA:3214Мальф.
Autosomal recessive

Deafness with labyrinthine aplasia, microtia, and microdontia

ORPHA:90024Мальф.
Autosomal recessive

Deafness-craniofacial syndrome

ORPHA:3241Мальф.

Deafness-ear malformation-facial palsy syndrome

ORPHA:3232Мальф.

Deafness-enamel hypoplasia-nail defects syndrome

ORPHA:3220Мальф.
Autosomal recessive

Deafness-epiphyseal dysplasia-short stature syndrome

ORPHA:3218Мальф.