MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
3,968 diseases matched (Disease) Reset

Congenital syphilis

ORPHA:499009Disease
Not applicable

Congenital thrombocytopenia-recurrent infections syndrome due to WIP deficiency

ORPHA:714493Disease
Autosomal recessive

Congenital toxoplasmosis

ORPHA:858Disease
Not applicable

Congenital trigeminal anesthesia

ORPHA:231013Disease
Not applicable

Congenital trochlear nerve palsy

ORPHA:98686Disease
Not applicable

Congenital tufting enteropathy

ORPHA:92050Disease
Autosomal recessive

Congenital varicella syndrome

ORPHA:291Disease
Not applicable

Conjunctival malignant melanoma

ORPHA:617910Disease

Connective tissue disorder due to lysyl hydroxylase-3 deficiency

ORPHA:300284Disease
Not applicable

Constitutional megaloblastic anemia with severe neurologic disease

ORPHA:319651Disease
Autosomal recessive

Constitutional mismatch repair deficiency syndrome

ORPHA:252202Disease
Autosomal recessive

Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome

ORPHA:352662Disease
Autosomal dominant

Corpus callosum agenesis-neuronopathy syndrome

ORPHA:1496Disease
Autosomal recessive

Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation

ORPHA:300570Disease
Autosomal dominant

Corticobasal syndrome

ORPHA:454887Disease

Corticosteroid-binding globulin deficiency

ORPHA:199247Disease
Semi-dominant

Coxopodopatellar syndrome

ORPHA:1509Disease
Autosomal dominant

Cramp-fasciculation syndrome

ORPHA:581271Disease
Autosomal dominant

Cranio-cervical dystonia with laryngeal and upper-limb involvement

ORPHA:420485Disease
Autosomal dominant

Craniofaciofrontodigital syndrome

ORPHA:363705Disease
Unknown

Craniopharyngioma

ORPHA:54595Disease
Not applicable

Creeping myiasis

ORPHA:504Disease
Not applicable

Crigler-Najjar syndrome

ORPHA:205Disease
Autosomal recessive

Crimean-Congo hemorrhagic fever

ORPHA:99827Disease