MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
218 diseases matched (Clin. grp.) Reset

Carcinoma of gallbladder and extrahepatic biliary tract

ORPHA:56044Clin. grp.
Not applicable

Central congenital hypothyroidism

ORPHA:226298Clin. grp.

Central nervous system embryonal tumor

ORPHA:251870Clin. grp.
Not applicable

Centronuclear myopathy

ORPHA:595Clin. grp.
Autosomal dominant, Autosomal recessive, X-linked recessive

Cephalocele

ORPHA:268817Clin. grp.

Cerebral cortical dysplasia

ORPHA:268950Clin. grp.

Charcot-Marie-Tooth disease type 1

ORPHA:65753Clin. grp.
Autosomal dominant

Charcot-Marie-Tooth disease type 4

ORPHA:64749Clin. grp.
Autosomal recessive

Choroid plexus tumor

ORPHA:251896Clin. grp.

Chronic cutaneous lupus erythematosus

ORPHA:163531Clin. grp.
Multigenic/multifactorial

Cleft lip with or without cleft palate

ORPHA:1991Clin. grp.

Cleft palate

ORPHA:2014Clin. grp.
Multigenic/multifactorial, Not applicable

Cobblestone lissencephaly

ORPHA:51577Clin. grp.
Autosomal recessive

Coenzyme Q10 deficiency

ORPHA:35656Clin. grp.
Autosomal recessive

Cold-induced sweating syndrome-hyperthermia spectrum

ORPHA:401993Clin. grp.
Autosomal recessive

Congenital adrenal hyperplasia

ORPHA:418Clin. grp.
Autosomal recessive

Congenital dyserythropoietic anemia

ORPHA:85Clin. grp.
Autosomal dominant, Autosomal recessive, X-linked recessive

Congenital isolated hyperinsulinism

ORPHA:657Clin. grp.
Autosomal dominant, Autosomal recessive

Congenital long QT syndrome

ORPHA:768Clin. grp.
Autosomal dominant, Autosomal recessive

Congenital myotonia

ORPHA:206973Clin. grp.

Congenital pulmonary veins atresia or stenosis

ORPHA:3188Clin. grp.
Not applicable

Congenital stationary night blindness

ORPHA:215Clin. grp.
Autosomal dominant, Autosomal recessive, X-linked recessive

Creatine deficiency syndrome

ORPHA:79172Clin. grp.
Autosomal recessive, Not applicable, X-linked recessive

Cutaneous mastocytosis

ORPHA:66646Clin. grp.
Not applicable