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7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
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8 700Фенотиптер
Табылды 727 заболеваний (Клин. под.) Қалпына келтіру

Acute endophthalmitis

ORPHA:279888Клин. под.
Not applicable

Acute mast cell leukemia

ORPHA:566393Клин. под.
Not applicable

Acute megakaryoblastic leukemia in children with Down syndrome

ORPHA:99887Клин. под.
Not applicable

Acute megakaryoblastic leukemia in children without Down syndrome

ORPHA:329469Клин. под.
Not applicable

Acute neonatal citrullinemia type I

ORPHA:247546Клин. под.
Autosomal recessive

Acute transverse myelitis with anti-MOG antibodies

ORPHA:592873Клин. под.

Adrenomyeloneuropathy

ORPHA:139399Клин. под.
X-linked recessive

Adult CLN1 disease

ORPHA:699745Клин. под.
Autosomal recessive

Adult CLN5 disease

ORPHA:699812Клин. под.
Autosomal recessive

Adult CLN6 disease

ORPHA:700477Клин. под.
Autosomal recessive

Adult Krabbe disease

ORPHA:206448Клин. под.
Autosomal recessive

Adult hypophosphatasia

ORPHA:247676Клин. под.
Autosomal dominant, Autosomal recessive

Adult intestinal botulism

ORPHA:178487Клин. под.

Adult polyglucosan body disease

ORPHA:206583Клин. под.
Autosomal recessive

Adult-onset Steinert myotonic dystrophy

ORPHA:589830Клин. под.
Autosomal dominant

Adult-onset myasthenia gravis

ORPHA:391490Клин. под.
Multigenic/multifactorial, Not applicable

Alexander disease type I

ORPHA:363717Клин. под.
Not applicable

Alexander disease type II

ORPHA:363722Клин. под.
Autosomal dominant

Alobar holoprosencephaly

ORPHA:93925Клин. под.
Multigenic/multifactorial, Not applicable

Alpha-N-acetylgalactosaminidase deficiency type 1

ORPHA:79279Клин. под.
Autosomal recessive

Alpha-N-acetylgalactosaminidase deficiency type 2

ORPHA:79280Клин. под.
Autosomal recessive

Alpha-N-acetylgalactosaminidase deficiency type 3

ORPHA:79281Клин. под.
Autosomal recessive

Alpha-heavy chain disease

ORPHA:100025Клин. под.

Alpha-mannosidosis, adult form

ORPHA:309288Клин. под.
Autosomal recessive