MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen

Complete hydatidiform mole

ORPHA:254688Kl. subt.
Autosomal recessive, Not applicable

Complex lethal osteochondrodysplasia

ORPHA:457378Malf.
Autosomal recessive

Complex regional pain syndrome

ORPHA:83452Kr.
Not applicable

Complex regional pain syndrome type 1

ORPHA:99995Kl. subt.

Complex regional pain syndrome type 2

ORPHA:99994Kl. subt.

Complication after organ transplantation

ORPHA:306644spez. Sit.
Not applicable

Complication in hemodialysis

ORPHA:268316spez. Sit.
Not applicable

Complications after hematopoietic stem cell transplantation

ORPHA:90053spez. Sit.
Not applicable

Composite hemangioendothelioma

ORPHA:458758Kr.
Not applicable

Composite lymphoma

ORPHA:168966Kr.

Conductive deafness-malformed external ear syndrome

ORPHA:3216Malf.
Unknown

Conductive deafness-ptosis-skeletal anomalies syndrome

ORPHA:3236Malf.

Cone dystrophy with supernormal rod response

ORPHA:209932Kr.
Autosomal recessive

Cone rod dystrophy

ORPHA:1872Kr.
Autosomal dominant, Autosomal recessive, X-linked recessive

Cone rod dystrophy-short stature syndrome

ORPHA:653709Kr.
Autosomal recessive

Confetti-like macular atrophy

ORPHA:221142Kr.

Congenital CLN10 disease

ORPHA:700487Kl. subt.
Autosomal recessive

Congenital Epstein-Barr virus infection

ORPHA:70596Kr.
Not applicable

Congenital Gerbode defect

ORPHA:99095Morph.

Congenital abducens nerve palsy

ORPHA:440233Kr.
Not applicable

Congenital achiasma

ORPHA:324353Morph.

Congenital adrenal hyperplasia

ORPHA:418Kl. gruppe
Autosomal recessive

Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency

ORPHA:90795Kr.
Autosomal recessive

Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency

ORPHA:90793Kr.
Autosomal recessive