MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Chondrosarcoma

ORPHA:55880Заболевание
Not applicable, Unknown

Chordoid glioma

ORPHA:251674Заболевание

Chordoma

ORPHA:178Заболевание
Autosomal dominant, Not applicable

Choreoacanthocytosis

ORPHA:2388Заболевание
Autosomal recessive

Choroid plexus carcinoma

ORPHA:251899Заболевание
Autosomal dominant

Choroid plexus tumor

ORPHA:251896Клин. группа

Choroidal atrophy-alopecia syndrome

ORPHA:1433Мальформация
Unknown

Choroidal osteoma

ORPHA:674965Заболевание

Choroideremia

ORPHA:180Заболевание
X-linked recessive

Christianson syndrome

ORPHA:85278Мальформация
X-linked recessive

Chromomycosis

ORPHA:182Заболевание
Not applicable

Chromophobe renal cell carcinoma

ORPHA:319303Заболевание

Chromosome Y microdeletion syndrome

ORPHA:1646Мальформация
Not applicable, Y-linked

Chronic Epstein-Barr virus infection syndrome

ORPHA:2566Заболевание
Unknown

Chronic actinic dermatitis

ORPHA:330064Заболевание
Not applicable

Chronic atrial and intestinal dysrhythmia syndrome

ORPHA:435988Заболевание
Autosomal recessive

Chronic beryllium disease

ORPHA:133Заболевание
Not applicable

Chronic bilirubin encephalopathy

ORPHA:529808Clinical syndrome
Not applicable

Chronic cutaneous lupus erythematosus

ORPHA:163531Клин. группа
Multigenic/multifactorial

Chronic diarrhea due to glucoamylase deficiency

ORPHA:103907Заболевание

Chronic diarrhea with villous atrophy

ORPHA:1670Заболевание

Chronic endophthalmitis

ORPHA:279891Клин. подтип
Not applicable

Chronic enteropathy associated with SLCO2A1 gene

ORPHA:468641Заболевание
Autosomal recessive

Chronic eosinophilic leukemia

ORPHA:168940Заболевание
Not applicable