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База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы
Найдено 1,772 заболеваний (Порок) Сброс

Crouzon syndrome-acanthosis nigricans syndrome

ORPHA:93262Порок
Autosomal dominant, Not applicable

Cryptomicrotia-brachydactyly-excess fingertip arch syndrome

ORPHA:1547Порок
Autosomal dominant

Cryptorchidism-arachnodactyly-intellectual disability syndrome

ORPHA:1548Порок

Currarino syndrome

ORPHA:1552Порок
Autosomal dominant, Not applicable

Curry-Jones syndrome

ORPHA:1553Порок
Not applicable

Cutaneous mastocytosis-deafness-microtia syndrome

ORPHA:2135Порок
Autosomal recessive

Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome

ORPHA:1555Порок
Autosomal dominant

Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies

ORPHA:221145Порок
Autosomal recessive

Cutis laxa-Marfanoid syndrome

ORPHA:171719Порок

Cutis marmorata telangiectatica congenita

ORPHA:1556Порок
Not applicable

Cyprus facial-neuromusculoskeletal syndrome

ORPHA:2674Порок
Autosomal dominant

Czeizel-Losonci syndrome

ORPHA:2437Порок
Autosomal dominant

DNMT3A-related microcephalic dwarfism

ORPHA:658595Порок
Autosomal dominant

DONSON-related microcephaly-short stature-limb abnormalities spectrum

ORPHA:572761Порок
Autosomal recessive

DOORS syndrome

ORPHA:79500Порок
Autosomal recessive

DYRK1A-related intellectual disability syndrome

ORPHA:464306Порок
Autosomal dominant, Not applicable, Unknown

Dahlberg-Borer-Newcomer syndrome

ORPHA:1563Порок
Autosomal recessive, X-linked recessive

Dandy-Walker malformation-postaxial polydactyly syndrome

ORPHA:1566Порок
Autosomal recessive

Deaf blind hypopigmentation syndrome, Yemenite type

ORPHA:3214Порок
Autosomal recessive

Deafness with labyrinthine aplasia, microtia, and microdontia

ORPHA:90024Порок
Autosomal recessive

Deafness-craniofacial syndrome

ORPHA:3241Порок

Deafness-ear malformation-facial palsy syndrome

ORPHA:3232Порок

Deafness-enamel hypoplasia-nail defects syndrome

ORPHA:3220Порок
Autosomal recessive

Deafness-epiphyseal dysplasia-short stature syndrome

ORPHA:3218Порок