Orphanet Database • Orphadata CC-BY-4.0
Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
7,547
Заболеваний
4 552
Генов
8 700
Фенотипов
140
Регионов
Все (7,547)Biological anomalyCategoryClinical groupClinical subtypeClinical syndromeDiseaseEtiological subtypeHistopathological subtypeMalformation syndromeMorphological anomalyParticular clinical situation in a disease or syndrome
ZMYND11-related developmental delay-speech delay-seizures-behavioral abnormalities-craniofacial dysmorphism syndrome
Autosomal dominant
Zebra body myopathy
Unknown
Neonatal
Zellweger syndrome
Autosomal recessive
Neonatal
Zellweger-like syndrome without peroxisomal anomalies
Autosomal recessive, Mitochondrial inheritance
Childhood
Zika virus disease
Not applicable
All ages
Zollinger-Ellison syndrome
Not applicable
Adult, Elderly
Zygomycosis
Not applicable
All ages
Åland Islands eye disease
X-linked recessive
Infancy, Neonatal