MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

Congenital syphilis

ORPHA:499009Kr.
Not applicable

Congenital thrombocytopenia-recurrent infections syndrome due to WIP deficiency

ORPHA:714493Kr.
Autosomal recessive

Congenital toxoplasmosis

ORPHA:858Kr.
Not applicable

Congenital trigeminal anesthesia

ORPHA:231013Kr.
Not applicable

Congenital trochlear nerve palsy

ORPHA:98686Kr.
Not applicable

Congenital tufting enteropathy

ORPHA:92050Kr.
Autosomal recessive

Congenital varicella syndrome

ORPHA:291Kr.
Not applicable

Conjunctival malignant melanoma

ORPHA:617910Kr.

Connective tissue disorder due to lysyl hydroxylase-3 deficiency

ORPHA:300284Kr.
Not applicable

Constitutional megaloblastic anemia with severe neurologic disease

ORPHA:319651Kr.
Autosomal recessive

Constitutional mismatch repair deficiency syndrome

ORPHA:252202Kr.
Autosomal recessive

Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome

ORPHA:352662Kr.
Autosomal dominant

Corpus callosum agenesis-neuronopathy syndrome

ORPHA:1496Kr.
Autosomal recessive

Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation

ORPHA:300570Kr.
Autosomal dominant

Corticobasal syndrome

ORPHA:454887Kr.

Corticosteroid-binding globulin deficiency

ORPHA:199247Kr.
Semi-dominant

Coxopodopatellar syndrome

ORPHA:1509Kr.
Autosomal dominant

Cramp-fasciculation syndrome

ORPHA:581271Kr.
Autosomal dominant

Cranio-cervical dystonia with laryngeal and upper-limb involvement

ORPHA:420485Kr.
Autosomal dominant

Craniofaciofrontodigital syndrome

ORPHA:363705Kr.
Unknown

Craniopharyngioma

ORPHA:54595Kr.
Not applicable

Creeping myiasis

ORPHA:504Kr.
Not applicable

Crigler-Najjar syndrome

ORPHA:205Kr.
Autosomal recessive

Crimean-Congo hemorrhagic fever

ORPHA:99827Kr.