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База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы
Найдено 727 заболеваний (Клин. подт.) Сброс

Acute endophthalmitis

ORPHA:279888Клин. подт.
Not applicable

Acute mast cell leukemia

ORPHA:566393Клин. подт.
Not applicable

Acute megakaryoblastic leukemia in children with Down syndrome

ORPHA:99887Клин. подт.
Not applicable

Acute megakaryoblastic leukemia in children without Down syndrome

ORPHA:329469Клин. подт.
Not applicable

Acute neonatal citrullinemia type I

ORPHA:247546Клин. подт.
Autosomal recessive

Acute transverse myelitis with anti-MOG antibodies

ORPHA:592873Клин. подт.

Adrenomyeloneuropathy

ORPHA:139399Клин. подт.
X-linked recessive

Adult CLN1 disease

ORPHA:699745Клин. подт.
Autosomal recessive

Adult CLN5 disease

ORPHA:699812Клин. подт.
Autosomal recessive

Adult CLN6 disease

ORPHA:700477Клин. подт.
Autosomal recessive

Adult Krabbe disease

ORPHA:206448Клин. подт.
Autosomal recessive

Adult hypophosphatasia

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

Adult intestinal botulism

ORPHA:178487Клин. подт.

Adult polyglucosan body disease

ORPHA:206583Клин. подт.
Autosomal recessive

Adult-onset Steinert myotonic dystrophy

ORPHA:589830Клин. подт.
Autosomal dominant

Adult-onset myasthenia gravis

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

Alexander disease type I

ORPHA:363717Клин. подт.
Not applicable

Alexander disease type II

ORPHA:363722Клин. подт.
Autosomal dominant

Alobar holoprosencephaly

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

Alpha-N-acetylgalactosaminidase deficiency type 1

ORPHA:79279Клин. подт.
Autosomal recessive

Alpha-N-acetylgalactosaminidase deficiency type 2

ORPHA:79280Клин. подт.
Autosomal recessive

Alpha-N-acetylgalactosaminidase deficiency type 3

ORPHA:79281Клин. подт.
Autosomal recessive

Alpha-heavy chain disease

ORPHA:100025Клин. подт.

Alpha-mannosidosis, adult form

ORPHA:309288Клин. подт.
Autosomal recessive