Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Hyperostosis corticalis generalisata
Autosomal dominant, Autosomal recessive
Adolescent, Childhood
Hyperostosis cranialis interna
Autosomal dominant
Adolescent, Adult, Childhood
Hyperparathyroidism-jaw tumor syndrome
Autosomal dominant
Adolescent, Adult
Hyperphenylalaninemia due to DNAJC12 deficiency
Autosomal recessive
Infancy
Hyperphenylalaninemia due to tetrahydrobiopterin deficiency
Autosomal recessive
Infancy, Neonatal
Hyperphosphatasia-intellectual disability syndrome
Autosomal recessive
Infancy, Neonatal
Hyperprolinemia type 1
Autosomal recessive
All ages
Hyperprolinemia type 2
Autosomal recessive
All ages
Hypersensitivity pneumonitis
Not applicable
All ages
Hypertelorism-hypospadias-polysyndactyly syndrome
Autosomal recessive
Neonatal
Hypertelorism-microtia-facial clefting syndrome
Autosomal recessive
Antenatal, Neonatal
Hypertelorism-preauricular sinus-punctual pits-deafness syndrome
Autosomal dominant
Infancy, Neonatal
Hypertrichosis cubiti
Autosomal dominant
Childhood
Hypertrichosis lanuginosa congenita
Autosomal dominant
Childhood
Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation
No data available
Infancy, Neonatal
Hypertrophic olivary degeneration
Hypertryptophanemia
Autosomal recessive
Childhood, Infancy, Neonatal
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome
Autosomal recessive
Infancy, Neonatal
Hyperzincemia and hypercalprotectinemia
Unknown
Childhood
Hypnic headache
Not applicable
Adult, Childhood, Elderly
Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome
Unknown
Infancy, Neonatal
Hypocalcemic vitamin D-dependent rickets
Autosomal recessive
Infancy, Neonatal
Hypocalcemic vitamin D-resistant rickets
Autosomal recessive
Infancy, Neonatal
Hypocalcified amelogenesis imperfecta
Autosomal dominant, Autosomal recessive