MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen

Chronic graft versus host disease

ORPHA:99921Kl. subt.

Chronic granulomatous disease

ORPHA:379Kr.
Autosomal recessive, X-linked recessive

Chronic hiccup

ORPHA:396Kr.
Not applicable

Chronic infantile diarrhea due to guanylate cyclase 2C overactivity

ORPHA:314373Kr.
Autosomal dominant

Chronic inflammatory demyelinating polyneuropathy

ORPHA:2932Kr.
Not applicable

Chronic intervillositis of unknown etiology

ORPHA:615970Kr.

Chronic intestinal failure

ORPHA:294422Clinical syndrome
Not applicable

Chronic intestinal pseudoobstruction syndrome

ORPHA:2978Clinical syndrome

Chronic lymphoproliferative disorder of natural killer cells

ORPHA:512017Kr.
Unknown

Chronic mast cell leukemia

ORPHA:566396Kl. subt.
Not applicable

Chronic mucocutaneous candidiasis

ORPHA:1334Kr.
Autosomal dominant, Autosomal recessive

Chronic myeloid leukemia

ORPHA:521Kr.
Not applicable

Chronic myelomonocytic leukemia

ORPHA:98823Kr.
Not applicable

Chronic myeloproliferative disease, unclassifiable

ORPHA:86830Kr.

Chronic neurovisceral acid sphingomyelinase deficiency

ORPHA:618891Kr.

Chronic neutrophilic leukemia

ORPHA:86829Kr.
Not applicable

Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis

ORPHA:324964Kr.
Not applicable

Chronic pneumonitis of infancy

ORPHA:91359Kr.
Not applicable

Chronic primary adrenal insufficiency

ORPHA:101959Kat.
Multigenic/multifactorial

Chronic respiratory distress with surfactant metabolism deficiency

ORPHA:217566Kr.
Autosomal dominant

Chronic thromboembolic pulmonary hypertension

ORPHA:70591Kr.
Not applicable

Chronic visceral acid sphingomyelinase deficiency

ORPHA:77293Kr.
Autosomal recessive

Chudley-McCullough syndrome

ORPHA:314597Malf.
Autosomal recessive

Chuvash erythrocytosis

ORPHA:238557Kr.
Autosomal recessive