Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
High-grade dysplasia in patients with Barrett esophagus
Not applicable
All ages
High-grade neuroendocrine carcinoma of the cervix uteri
Adult, Elderly
Hinman syndrome
All ages
Hip dysplasia, Beukes type
Autosomal dominant
Childhood
Hirschsprung disease
Autosomal dominant, Autosomal recessive, Multigenic/multifactorial, Not applicable
Childhood, Infancy, Neonatal
Hirschsprung disease-deafness-polydactyly syndrome
Autosomal recessive
Neonatal
Hirschsprung disease-ganglioneuroblastoma syndrome
Neonatal
Hirschsprung disease-nail hypoplasia-dysmorphism syndrome
Autosomal recessive
Neonatal
Hirschsprung disease-type D brachydactyly syndrome
Neonatal
His bundle tachycardia
Unknown
Infancy, Neonatal
Histidinemia
Autosomal recessive
Infancy, Neonatal
Histidinuria-renal tubular defect syndrome
Childhood, Infancy
Histiocytic and dendritic cell tumor
Histiocytic sarcoma
Adult
Histiocytoid cardiomyopathy
Autosomal recessive, Unknown, X-linked dominant
Infancy, Neonatal
Hobnail hemangioma
All ages
Hodgkin lymphoma
Multigenic/multifactorial
Adolescent, Adult, Childhood, Elderly, Infancy
Holmes-Adie syndrome
Not applicable
Adult
Holocarboxylase synthetase deficiency
Autosomal recessive
Childhood, Infancy, Neonatal
Holoprosencephaly
Autosomal recessive, Multigenic/multifactorial, Not applicable, Oligogenic, X-linked dominant
Antenatal, Neonatal
Holoprosencephaly-caudal dysgenesis syndrome
Antenatal, Neonatal
Holoprosencephaly-craniosynostosis syndrome
Antenatal, Neonatal
Holoprosencephaly-postaxial polydactyly syndrome
Autosomal recessive
Antenatal, Neonatal
Holoprosencephaly-radial heart renal anomalies syndrome
Antenatal, Neonatal