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Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер
Табылды 3,968 заболеваний (Ауру) Қалпына келтіру

Hereditary sensory and autonomic neuropathy type 7

ORPHA:391397Ауру
Autosomal dominant

Hereditary sensory and autonomic neuropathy type 8

ORPHA:478664Ауру
Autosomal recessive

Hereditary sensory and autonomic neuropathy with deafness and global delay

ORPHA:139573Ауру
Autosomal recessive

Hereditary sensory neuropathy-deafness-dementia syndrome

ORPHA:456318Ауру
Autosomal dominant

Hereditary sick sinus syndrome

ORPHA:166282Ауру
Autosomal dominant, Autosomal recessive

Hereditary sodium channelopathy-related small fibers neuropathy

ORPHA:306577Ауру
Autosomal dominant

Hereditary spherocytosis

ORPHA:822Ауру
Autosomal dominant, Autosomal recessive

Hereditary steroid-resistant nephrotic syndrome

ORPHA:656Ауру
Autosomal dominant, Autosomal recessive

Hereditary thermosensitive neuropathy

ORPHA:84093Ауру

Hereditary thrombocytopenia with early-onset myelofibrosis

ORPHA:480851Ауру
Autosomal dominant

Hereditary thrombocytopenia with normal platelets

ORPHA:268322Ауру
Autosomal dominant, Autosomal recessive, X-linked recessive

Hereditary thrombophilia due to congenital antithrombin deficiency

ORPHA:82Ауру
Autosomal dominant

Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency

ORPHA:217467Ауру
Autosomal dominant

Hereditary xanthinuria

ORPHA:3467Ауру
Autosomal recessive

Hermansky-Pudlak syndrome

ORPHA:79430Ауру
Autosomal recessive

Herpes simplex virus encephalitis

ORPHA:1930Ауру
Multigenic/multifactorial, Not applicable

Herpes simplex virus stromal keratitis

ORPHA:137599Ауру
Not applicable

Heterozygous beta-thalassemia intermedia with supernumerary alpha-globin gene

ORPHA:715143Ауру
Autosomal recessive

Hidrotic ectodermal dysplasia

ORPHA:189Ауру
Autosomal dominant

High bone mass osteogenesis imperfecta

ORPHA:314029Ауру
Autosomal dominant

High grade B-cell lymphoma with MYC and/ or BCL2 and/or BCL6 rearrangement

ORPHA:480541Ауру

High myopia-sensorineural deafness syndrome

ORPHA:363396Ауру
Autosomal recessive

High-grade neuroendocrine carcinoma of the cervix uteri

ORPHA:213777Ауру

Hinman syndrome

ORPHA:84085Ауру