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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Complete hydatidiform mole

ORPHA:254688Clin. sub.
Autosomal recessive, Not applicable

Complex lethal osteochondrodysplasia

ORPHA:457378Malform.
Autosomal recessive

Complex regional pain syndrome

ORPHA:83452Disease
Not applicable

Complex regional pain syndrome type 1

ORPHA:99995Clin. sub.

Complex regional pain syndrome type 2

ORPHA:99994Clin. sub.

Complication after organ transplantation

ORPHA:306644Situation
Not applicable

Complication in hemodialysis

ORPHA:268316Situation
Not applicable

Complications after hematopoietic stem cell transplantation

ORPHA:90053Situation
Not applicable

Composite hemangioendothelioma

ORPHA:458758Disease
Not applicable

Composite lymphoma

ORPHA:168966Disease

Conductive deafness-malformed external ear syndrome

ORPHA:3216Malform.
Unknown

Conductive deafness-ptosis-skeletal anomalies syndrome

ORPHA:3236Malform.

Cone dystrophy with supernormal rod response

ORPHA:209932Disease
Autosomal recessive

Cone rod dystrophy

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

Cone rod dystrophy-short stature syndrome

ORPHA:653709Disease
Autosomal recessive

Confetti-like macular atrophy

ORPHA:221142Disease

Congenital CLN10 disease

ORPHA:700487Clin. sub.
Autosomal recessive

Congenital Epstein-Barr virus infection

ORPHA:70596Disease
Not applicable

Congenital Gerbode defect

ORPHA:99095Morph.

Congenital abducens nerve palsy

ORPHA:440233Disease
Not applicable

Congenital achiasma

ORPHA:324353Morph.

Congenital adrenal hyperplasia

ORPHA:418Clin. grp.
Autosomal recessive

Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency

ORPHA:90795Disease
Autosomal recessive

Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency

ORPHA:90793Disease
Autosomal recessive