MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Chronic graft versus host disease

ORPHA:99921Клин. подтип

Chronic granulomatous disease

ORPHA:379Заболевание
Autosomal recessive, X-linked recessive

Chronic hiccup

ORPHA:396Заболевание
Not applicable

Chronic infantile diarrhea due to guanylate cyclase 2C overactivity

ORPHA:314373Заболевание
Autosomal dominant

Chronic inflammatory demyelinating polyneuropathy

ORPHA:2932Заболевание
Not applicable

Chronic intervillositis of unknown etiology

ORPHA:615970Заболевание

Chronic intestinal failure

ORPHA:294422Clinical syndrome
Not applicable

Chronic intestinal pseudoobstruction syndrome

ORPHA:2978Clinical syndrome

Chronic lymphoproliferative disorder of natural killer cells

ORPHA:512017Заболевание
Unknown

Chronic mast cell leukemia

ORPHA:566396Клин. подтип
Not applicable

Chronic mucocutaneous candidiasis

ORPHA:1334Заболевание
Autosomal dominant, Autosomal recessive

Chronic myeloid leukemia

ORPHA:521Заболевание
Not applicable

Chronic myelomonocytic leukemia

ORPHA:98823Заболевание
Not applicable

Chronic myeloproliferative disease, unclassifiable

ORPHA:86830Заболевание

Chronic neurovisceral acid sphingomyelinase deficiency

ORPHA:618891Заболевание

Chronic neutrophilic leukemia

ORPHA:86829Заболевание
Not applicable

Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis

ORPHA:324964Заболевание
Not applicable

Chronic pneumonitis of infancy

ORPHA:91359Заболевание
Not applicable

Chronic primary adrenal insufficiency

ORPHA:101959Категория
Multigenic/multifactorial

Chronic respiratory distress with surfactant metabolism deficiency

ORPHA:217566Заболевание
Autosomal dominant

Chronic thromboembolic pulmonary hypertension

ORPHA:70591Заболевание
Not applicable

Chronic visceral acid sphingomyelinase deficiency

ORPHA:77293Заболевание
Autosomal recessive

Chudley-McCullough syndrome

ORPHA:314597Мальформация
Autosomal recessive

Chuvash erythrocytosis

ORPHA:238557Заболевание
Autosomal recessive