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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

H syndrome

ORPHA:168569Мальф.
Autosomal recessive

HANAC syndrome

ORPHA:73229Ауру
Autosomal dominant

HEC syndrome

ORPHA:2119Мальф.
Unknown

HELLP syndrome

ORPHA:244242Ауру
Multigenic/multifactorial

HHV-8-associated multicentric Castleman disease

ORPHA:570438Клин. под.

HIDEA syndrome

ORPHA:436141Мальф.
Autosomal recessive

HIV-associated cancer

ORPHA:443291Жағдай
Not applicable

HJV or HAMP-related hemochromatosis

ORPHA:79230Ауру
Autosomal recessive

HNF1B-related autosomal dominant tubulointerstitial kidney disease

ORPHA:93111Клин. под.
Autosomal dominant

HNRNPA1-related adult-onset distal myopathy

ORPHA:399086Ауру

HNRNPDL-related limb-girdle muscular dystrophy D3

ORPHA:55596Ауру
Autosomal dominant

HSD10 disease

ORPHA:391417Ауру
X-linked dominant

HSD10 disease, atypical type

ORPHA:85295Клин. под.
X-linked dominant

HSD10 disease, infantile type

ORPHA:391428Клин. под.
X-linked dominant

HSD10 disease, neonatal type

ORPHA:391457Клин. под.
X-linked dominant

HSPB8-related autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome

ORPHA:476093Ауру
Autosomal dominant

HTRA1-related autosomal dominant cerebral small vessel disease

ORPHA:482077Ауру
Autosomal dominant

Haddad syndrome

ORPHA:99803Мальф.
Autosomal dominant, Multigenic/multifactorial

Hailey-Hailey disease

ORPHA:2841Ауру
Autosomal dominant

Haim-Munk syndrome

ORPHA:2342Ауру
Autosomal recessive

Hairy cell leukemia variant

ORPHA:300878Ауру
Unknown

Hajdu-Cheney syndrome

ORPHA:955Мальф.
Autosomal dominant

Hall-Riggs syndrome

ORPHA:2107Мальф.
Autosomal recessive

Hallermann-Streiff syndrome

ORPHA:2108Мальф.
Not applicable, Unknown