Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Chondrosarcoma
Not applicable, Unknown
Adult
Chordoid glioma
Adult
Chordoma
Autosomal dominant, Not applicable
Adult
Choreoacanthocytosis
Autosomal recessive
Adult
Choroid plexus carcinoma
Autosomal dominant
Childhood
Choroid plexus tumor
Choroidal atrophy-alopecia syndrome
Unknown
Neonatal
Choroidal osteoma
All ages
Choroideremia
X-linked recessive
Adolescent, Adult, Childhood
Christianson syndrome
X-linked recessive
Infancy, Neonatal
Chromomycosis
Not applicable
All ages
Chromophobe renal cell carcinoma
Adult, Elderly
Chromosome Y microdeletion syndrome
Not applicable, Y-linked
Adult
Chronic Epstein-Barr virus infection syndrome
Unknown
Adolescent, Adult, Childhood
Chronic actinic dermatitis
Not applicable
Adult
Chronic atrial and intestinal dysrhythmia syndrome
Autosomal recessive
Adolescent, Adult, Childhood
Chronic beryllium disease
Not applicable
Adult
Chronic bilirubin encephalopathy
Not applicable
Infancy, Neonatal
Chronic cutaneous lupus erythematosus
Multigenic/multifactorial
Adolescent, Adult, Childhood, Elderly
Chronic diarrhea due to glucoamylase deficiency
Childhood
Chronic diarrhea with villous atrophy
Infancy
Chronic endophthalmitis
Not applicable
All ages
Chronic enteropathy associated with SLCO2A1 gene
Autosomal recessive
Adolescent, Adult, Childhood
Chronic eosinophilic leukemia
Not applicable
Adolescent, Adult, Childhood