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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Complete hydatidiform mole

ORPHA:254688Клин. под.
Autosomal recessive, Not applicable

Complex lethal osteochondrodysplasia

ORPHA:457378Мальф.
Autosomal recessive

Complex regional pain syndrome

ORPHA:83452Ауру
Not applicable

Complex regional pain syndrome type 1

ORPHA:99995Клин. под.

Complex regional pain syndrome type 2

ORPHA:99994Клин. под.

Complication after organ transplantation

ORPHA:306644Жағдай
Not applicable

Complication in hemodialysis

ORPHA:268316Жағдай
Not applicable

Complications after hematopoietic stem cell transplantation

ORPHA:90053Жағдай
Not applicable

Composite hemangioendothelioma

ORPHA:458758Ауру
Not applicable

Composite lymphoma

ORPHA:168966Ауру

Conductive deafness-malformed external ear syndrome

ORPHA:3216Мальф.
Unknown

Conductive deafness-ptosis-skeletal anomalies syndrome

ORPHA:3236Мальф.

Cone dystrophy with supernormal rod response

ORPHA:209932Ауру
Autosomal recessive

Cone rod dystrophy

ORPHA:1872Ауру
Autosomal dominant, Autosomal recessive, X-linked recessive

Cone rod dystrophy-short stature syndrome

ORPHA:653709Ауру
Autosomal recessive

Confetti-like macular atrophy

ORPHA:221142Ауру

Congenital CLN10 disease

ORPHA:700487Клин. под.
Autosomal recessive

Congenital Epstein-Barr virus infection

ORPHA:70596Ауру
Not applicable

Congenital Gerbode defect

ORPHA:99095Морф.

Congenital abducens nerve palsy

ORPHA:440233Ауру
Not applicable

Congenital achiasma

ORPHA:324353Морф.

Congenital adrenal hyperplasia

ORPHA:418Клин. топ
Autosomal recessive

Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency

ORPHA:90795Ауру
Autosomal recessive

Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency

ORPHA:90793Ауру
Autosomal recessive