MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
727 Erkrankungen gefunden (Kl. subt.) Zurücksetzen

Choanal atresia, bilateral

ORPHA:137920Kl. subt.
Not applicable

Choanal atresia, unilateral

ORPHA:137917Kl. subt.
Not applicable

Cholesteryl ester storage disease

ORPHA:75234Kl. subt.
Autosomal recessive

Chronic endophthalmitis

ORPHA:279891Kl. subt.
Not applicable

Chronic graft versus host disease

ORPHA:99921Kl. subt.

Chronic mast cell leukemia

ORPHA:566396Kl. subt.
Not applicable

Classic bladder exstrophy

ORPHA:93930Kl. subt.
Multigenic/multifactorial

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

ORPHA:315306Kl. subt.
Autosomal recessive

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

ORPHA:315311Kl. subt.
Autosomal recessive

Classic congenital lipoid adrenal hyperplasia due to STAR deficency

ORPHA:325524Kl. subt.
Autosomal recessive

Classic maple syrup urine disease

ORPHA:268145Kl. subt.
Autosomal recessive

Classic multiminicore myopathy

ORPHA:324604Kl. subt.
Autosomal recessive

Classic neuroendocrine tumor of appendix

ORPHA:329977Kl. subt.
Not applicable

Classic pantothenate kinase-associated neurodegeneration

ORPHA:216866Kl. subt.
Autosomal recessive

Classic progressive supranuclear palsy syndrome

ORPHA:240071Kl. subt.
Not applicable

Classic pyoderma gangrenosum

ORPHA:538863Kl. subt.
Multigenic/multifactorial

Classic stiff person syndrome

ORPHA:443192Kl. subt.
Not applicable

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

ORPHA:261190Kl. subt.
Not applicable, Unknown

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

ORPHA:652514Kl. subt.
Autosomal dominant

Cloacal exstrophy

ORPHA:93929Kl. subt.
Multigenic/multifactorial

Closed iniencephaly

ORPHA:268366Kl. subt.
Multigenic/multifactorial, Not applicable

Cockayne syndrome type 1

ORPHA:90321Kl. subt.
Autosomal recessive

Cockayne syndrome type 2

ORPHA:90322Kl. subt.
Autosomal recessive

Cockayne syndrome type 3

ORPHA:90324Kl. subt.
Autosomal recessive