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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы
Найдено 727 заболеваний (Клин. подт.) Сброс

Choanal atresia, bilateral

ORPHA:137920Клин. подт.
Not applicable

Choanal atresia, unilateral

ORPHA:137917Клин. подт.
Not applicable

Cholesteryl ester storage disease

ORPHA:75234Клин. подт.
Autosomal recessive

Chronic endophthalmitis

ORPHA:279891Клин. подт.
Not applicable

Chronic graft versus host disease

ORPHA:99921Клин. подт.

Chronic mast cell leukemia

ORPHA:566396Клин. подт.
Not applicable

Classic bladder exstrophy

ORPHA:93930Клин. подт.
Multigenic/multifactorial

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

ORPHA:315306Клин. подт.
Autosomal recessive

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

ORPHA:315311Клин. подт.
Autosomal recessive

Classic congenital lipoid adrenal hyperplasia due to STAR deficency

ORPHA:325524Клин. подт.
Autosomal recessive

Classic maple syrup urine disease

ORPHA:268145Клин. подт.
Autosomal recessive

Classic multiminicore myopathy

ORPHA:324604Клин. подт.
Autosomal recessive

Classic neuroendocrine tumor of appendix

ORPHA:329977Клин. подт.
Not applicable

Classic pantothenate kinase-associated neurodegeneration

ORPHA:216866Клин. подт.
Autosomal recessive

Classic progressive supranuclear palsy syndrome

ORPHA:240071Клин. подт.
Not applicable

Classic pyoderma gangrenosum

ORPHA:538863Клин. подт.
Multigenic/multifactorial

Classic stiff person syndrome

ORPHA:443192Клин. подт.
Not applicable

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

ORPHA:261190Клин. подт.
Not applicable, Unknown

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

ORPHA:652514Клин. подт.
Autosomal dominant

Cloacal exstrophy

ORPHA:93929Клин. подт.
Multigenic/multifactorial

Closed iniencephaly

ORPHA:268366Клин. подт.
Multigenic/multifactorial, Not applicable

Cockayne syndrome type 1

ORPHA:90321Клин. подт.
Autosomal recessive

Cockayne syndrome type 2

ORPHA:90322Клин. подт.
Autosomal recessive

Cockayne syndrome type 3

ORPHA:90324Клин. подт.
Autosomal recessive