MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Hyperostosis corticalis generalisata

ORPHA:3416Мальформация
Autosomal dominant, Autosomal recessive

Hyperostosis cranialis interna

ORPHA:443098Заболевание
Autosomal dominant

Hyperparathyroidism-jaw tumor syndrome

ORPHA:99880Заболевание
Autosomal dominant

Hyperphenylalaninemia due to DNAJC12 deficiency

ORPHA:508523Заболевание
Autosomal recessive

Hyperphenylalaninemia due to tetrahydrobiopterin deficiency

ORPHA:238583Заболевание
Autosomal recessive

Hyperphosphatasia-intellectual disability syndrome

ORPHA:247262Заболевание
Autosomal recessive

Hyperprolinemia type 1

ORPHA:419Заболевание
Autosomal recessive

Hyperprolinemia type 2

ORPHA:79101Заболевание
Autosomal recessive

Hypersensitivity pneumonitis

ORPHA:31740Заболевание
Not applicable

Hypertelorism-hypospadias-polysyndactyly syndrome

ORPHA:2211Мальформация
Autosomal recessive

Hypertelorism-microtia-facial clefting syndrome

ORPHA:2213Мальформация
Autosomal recessive

Hypertelorism-preauricular sinus-punctual pits-deafness syndrome

ORPHA:293958Мальформация
Autosomal dominant

Hypertrichosis cubiti

ORPHA:2220Мальформация
Autosomal dominant

Hypertrichosis lanuginosa congenita

ORPHA:2222Заболевание
Autosomal dominant

Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation

ORPHA:324525Заболевание
No data available

Hypertrophic olivary degeneration

ORPHA:684290Заболевание

Hypertryptophanemia

ORPHA:2224Заболевание
Autosomal recessive

Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome

ORPHA:363694Заболевание
Autosomal recessive

Hyperzincemia and hypercalprotectinemia

ORPHA:251523Заболевание
Unknown

Hypnic headache

ORPHA:276429Заболевание
Not applicable

Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome

ORPHA:2435Заболевание
Unknown

Hypocalcemic vitamin D-dependent rickets

ORPHA:289157Заболевание
Autosomal recessive

Hypocalcemic vitamin D-resistant rickets

ORPHA:93160Заболевание
Autosomal recessive

Hypocalcified amelogenesis imperfecta

ORPHA:100032Клин. подтип
Autosomal dominant, Autosomal recessive