Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Helsmoortel-Van der Aa syndrome
Unknown
Childhood, Infancy
Hemangioblastoma
Adult
Heme oxygenase-1 deficiency
Autosomal recessive
Adolescent, Childhood
Hemicrania continua
Not applicable
Hemidystonia-hemiatrophy syndrome
Not applicable
Adolescent, Adult, Childhood, Infancy, Neonatal
Hemifacial hyperplasia
Not applicable
Antenatal, Infancy, Neonatal
Hemifacial myohyperplasia
Neonatal
Hemifacial spasm
Adult, Elderly
Hemihyperplasia-multiple lipomatosis syndrome
Not applicable
Childhood
Hemimegalencephaly
Not applicable
Infancy
Hemiparkinsonism-hemiatrophy syndrome
Adolescent, Adult
Hemoglobin Bart's fetalis syndrome
Autosomal recessive
Antenatal, Neonatal
Hemoglobin C disease
Autosomal recessive
All ages
Hemoglobin C-beta-thalassemia syndrome
Autosomal recessive
Adolescent, Adult, Childhood, Infancy
Hemoglobin D disease
Autosomal recessive
Childhood
Hemoglobin E disease
Autosomal recessive
All ages
Hemoglobin E-beta-thalassemia intermedia
Autosomal recessive
Hemoglobin E-beta-thalassemia major
Autosomal recessive
Hemoglobin E-beta-thalassemia syndrome
Autosomal recessive
Adolescent, Adult, Childhood, Infancy
Hemoglobin H disease
Autosomal recessive
All ages
Hemoglobin Lepore-beta-thalassemia intermedia
Autosomal recessive
Hemoglobin Lepore-beta-thalassemia major
Autosomal recessive
Hemoglobin Lepore-beta-thalassemia syndrome
Autosomal recessive
No data available
Hemoglobin M disease
Autosomal dominant
No data available