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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Hyperostosis corticalis generalisata

ORPHA:3416Мальф.
Autosomal dominant, Autosomal recessive

Hyperostosis cranialis interna

ORPHA:443098Ауру
Autosomal dominant

Hyperparathyroidism-jaw tumor syndrome

ORPHA:99880Ауру
Autosomal dominant

Hyperphenylalaninemia due to DNAJC12 deficiency

ORPHA:508523Ауру
Autosomal recessive

Hyperphenylalaninemia due to tetrahydrobiopterin deficiency

ORPHA:238583Ауру
Autosomal recessive

Hyperphosphatasia-intellectual disability syndrome

ORPHA:247262Ауру
Autosomal recessive

Hyperprolinemia type 1

ORPHA:419Ауру
Autosomal recessive

Hyperprolinemia type 2

ORPHA:79101Ауру
Autosomal recessive

Hypersensitivity pneumonitis

ORPHA:31740Ауру
Not applicable

Hypertelorism-hypospadias-polysyndactyly syndrome

ORPHA:2211Мальф.
Autosomal recessive

Hypertelorism-microtia-facial clefting syndrome

ORPHA:2213Мальф.
Autosomal recessive

Hypertelorism-preauricular sinus-punctual pits-deafness syndrome

ORPHA:293958Мальф.
Autosomal dominant

Hypertrichosis cubiti

ORPHA:2220Мальф.
Autosomal dominant

Hypertrichosis lanuginosa congenita

ORPHA:2222Ауру
Autosomal dominant

Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation

ORPHA:324525Ауру
No data available

Hypertrophic olivary degeneration

ORPHA:684290Ауру

Hypertryptophanemia

ORPHA:2224Ауру
Autosomal recessive

Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome

ORPHA:363694Ауру
Autosomal recessive

Hyperzincemia and hypercalprotectinemia

ORPHA:251523Ауру
Unknown

Hypnic headache

ORPHA:276429Ауру
Not applicable

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

ORPHA:2435Ауру
Unknown

Hypocalcemic vitamin D-dependent rickets

ORPHA:289157Ауру
Autosomal recessive

Hypocalcemic vitamin D-resistant rickets

ORPHA:93160Ауру
Autosomal recessive

Hypocalcified amelogenesis imperfecta

ORPHA:100032Клин. под.
Autosomal dominant, Autosomal recessive