MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
1,772 Erkrankungen gefunden (Malf.) Zurücksetzen

Crouzon syndrome-acanthosis nigricans syndrome

ORPHA:93262Malf.
Autosomal dominant, Not applicable

Cryptomicrotia-brachydactyly-excess fingertip arch syndrome

ORPHA:1547Malf.
Autosomal dominant

Cryptorchidism-arachnodactyly-intellectual disability syndrome

ORPHA:1548Malf.

Currarino syndrome

ORPHA:1552Malf.
Autosomal dominant, Not applicable

Curry-Jones syndrome

ORPHA:1553Malf.
Not applicable

Cutaneous mastocytosis-deafness-microtia syndrome

ORPHA:2135Malf.
Autosomal recessive

Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome

ORPHA:1555Malf.
Autosomal dominant

Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies

ORPHA:221145Malf.
Autosomal recessive

Cutis laxa-Marfanoid syndrome

ORPHA:171719Malf.

Cutis marmorata telangiectatica congenita

ORPHA:1556Malf.
Not applicable

Cyprus facial-neuromusculoskeletal syndrome

ORPHA:2674Malf.
Autosomal dominant

Czeizel-Losonci syndrome

ORPHA:2437Malf.
Autosomal dominant

DNMT3A-related microcephalic dwarfism

ORPHA:658595Malf.
Autosomal dominant

DONSON-related microcephaly-short stature-limb abnormalities spectrum

ORPHA:572761Malf.
Autosomal recessive

DOORS syndrome

ORPHA:79500Malf.
Autosomal recessive

DYRK1A-related intellectual disability syndrome

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

Dahlberg-Borer-Newcomer syndrome

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

Dandy-Walker malformation-postaxial polydactyly syndrome

ORPHA:1566Malf.
Autosomal recessive

Deaf blind hypopigmentation syndrome, Yemenite type

ORPHA:3214Malf.
Autosomal recessive

Deafness with labyrinthine aplasia, microtia, and microdontia

ORPHA:90024Malf.
Autosomal recessive

Deafness-craniofacial syndrome

ORPHA:3241Malf.

Deafness-ear malformation-facial palsy syndrome

ORPHA:3232Malf.

Deafness-enamel hypoplasia-nail defects syndrome

ORPHA:3220Malf.
Autosomal recessive

Deafness-epiphyseal dysplasia-short stature syndrome

ORPHA:3218Malf.