MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

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

Choanal atresia, bilateral

ORPHA:137920Clin. sub.
Not applicable

Choanal atresia, unilateral

ORPHA:137917Clin. sub.
Not applicable

Cholesteryl ester storage disease

ORPHA:75234Clin. sub.
Autosomal recessive

Chronic endophthalmitis

ORPHA:279891Clin. sub.
Not applicable

Chronic graft versus host disease

ORPHA:99921Clin. sub.

Chronic mast cell leukemia

ORPHA:566396Clin. sub.
Not applicable

Classic bladder exstrophy

ORPHA:93930Clin. sub.
Multigenic/multifactorial

Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form

ORPHA:315306Clin. sub.
Autosomal recessive

Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form

ORPHA:315311Clin. sub.
Autosomal recessive

Classic congenital lipoid adrenal hyperplasia due to STAR deficency

ORPHA:325524Clin. sub.
Autosomal recessive

Classic maple syrup urine disease

ORPHA:268145Clin. sub.
Autosomal recessive

Classic multiminicore myopathy

ORPHA:324604Clin. sub.
Autosomal recessive

Classic neuroendocrine tumor of appendix

ORPHA:329977Clin. sub.
Not applicable

Classic pantothenate kinase-associated neurodegeneration

ORPHA:216866Clin. sub.
Autosomal recessive

Classic progressive supranuclear palsy syndrome

ORPHA:240071Clin. sub.
Not applicable

Classic pyoderma gangrenosum

ORPHA:538863Clin. sub.
Multigenic/multifactorial

Classic stiff person syndrome

ORPHA:443192Clin. sub.
Not applicable

Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion

ORPHA:261190Clin. sub.
Not applicable, Unknown

Cleft palate-congenital heart defect-intellectual disability syndrome due to MEIS2 mutation

ORPHA:652514Clin. sub.
Autosomal dominant

Cloacal exstrophy

ORPHA:93929Clin. sub.
Multigenic/multifactorial

Closed iniencephaly

ORPHA:268366Clin. sub.
Multigenic/multifactorial, Not applicable

Cockayne syndrome type 1

ORPHA:90321Clin. sub.
Autosomal recessive

Cockayne syndrome type 2

ORPHA:90322Clin. sub.
Autosomal recessive

Cockayne syndrome type 3

ORPHA:90324Clin. sub.
Autosomal recessive