MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen

Classic hairy cell leukemia

ORPHA:58017Kr.
Unknown

Classic heparin-induced thrombocytopenia

ORPHA:3325Kr.
Not applicable

Classic maple syrup urine disease

ORPHA:268145Kl. subt.
Autosomal recessive

Classic medulloblastoma

ORPHA:251867His. subt.

Classic multiminicore myopathy

ORPHA:324604Kl. subt.
Autosomal recessive

Classic mycosis fungoides

ORPHA:2584Kr.
Multigenic/multifactorial, Not applicable

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

Classical Ehlers-Danlos syndrome

ORPHA:287Kr.
Autosomal dominant

Classical-like Ehlers-Danlos syndrome type 1

ORPHA:230839Kr.
Autosomal recessive

Classical-like Ehlers-Danlos syndrome type 2

ORPHA:536532Kr.
Autosomal recessive

Clear cell adenocarcinoma of the ovary

ORPHA:398971Kr.

Clear cell papillary renal cell carcinoma

ORPHA:404511His. subt.

Clear cell renal carcinoma

ORPHA:319276Kr.
Not applicable

Clear cell sarcoma of kidney

ORPHA:457246Kr.
Not applicable

Cleft hard palate

ORPHA:101023Morph.

Cleft lip and alveolus

ORPHA:141291Morph.
Multigenic/multifactorial

Cleft lip and palate-craniofacial dysmorphism-congenital heart defect-hearing loss syndrome

ORPHA:508476Malf.
Autosomal recessive

Cleft lip with or without cleft palate

ORPHA:1991Kl. gruppe

Cleft lip/palate

ORPHA:199306Morph.
Multigenic/multifactorial

Cleft lip/palate-deafness-sacral lipoma syndrome

ORPHA:2003Malf.
Unknown