MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
1,772 diseases matched (Malform.) Reset

Crouzon syndrome-acanthosis nigricans syndrome

ORPHA:93262Malform.
Autosomal dominant, Not applicable

Cryptomicrotia-brachydactyly-excess fingertip arch syndrome

ORPHA:1547Malform.
Autosomal dominant

Cryptorchidism-arachnodactyly-intellectual disability syndrome

ORPHA:1548Malform.

Currarino syndrome

ORPHA:1552Malform.
Autosomal dominant, Not applicable

Curry-Jones syndrome

ORPHA:1553Malform.
Not applicable

Cutaneous mastocytosis-deafness-microtia syndrome

ORPHA:2135Malform.
Autosomal recessive

Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome

ORPHA:1555Malform.
Autosomal dominant

Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies

ORPHA:221145Malform.
Autosomal recessive

Cutis laxa-Marfanoid syndrome

ORPHA:171719Malform.

Cutis marmorata telangiectatica congenita

ORPHA:1556Malform.
Not applicable

Cyprus facial-neuromusculoskeletal syndrome

ORPHA:2674Malform.
Autosomal dominant

Czeizel-Losonci syndrome

ORPHA:2437Malform.
Autosomal dominant

DNMT3A-related microcephalic dwarfism

ORPHA:658595Malform.
Autosomal dominant

DONSON-related microcephaly-short stature-limb abnormalities spectrum

ORPHA:572761Malform.
Autosomal recessive

DOORS syndrome

ORPHA:79500Malform.
Autosomal recessive

DYRK1A-related intellectual disability syndrome

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

Dahlberg-Borer-Newcomer syndrome

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

Dandy-Walker malformation-postaxial polydactyly syndrome

ORPHA:1566Malform.
Autosomal recessive

Deaf blind hypopigmentation syndrome, Yemenite type

ORPHA:3214Malform.
Autosomal recessive

Deafness with labyrinthine aplasia, microtia, and microdontia

ORPHA:90024Malform.
Autosomal recessive

Deafness-craniofacial syndrome

ORPHA:3241Malform.

Deafness-ear malformation-facial palsy syndrome

ORPHA:3232Malform.

Deafness-enamel hypoplasia-nail defects syndrome

ORPHA:3220Malform.
Autosomal recessive

Deafness-epiphyseal dysplasia-short stature syndrome

ORPHA:3218Malform.