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База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы

Accessory pancreas

ORPHA:674Морф.
Not applicable

Aceruloplasminemia

ORPHA:48818Заболевание
Autosomal recessive

Acetazolamide-responsive myotonia

ORPHA:99736Заболевание
Autosomal dominant

Achalasia-microcephaly syndrome

ORPHA:929Порок
Autosomal recessive

Achondrogenesis

ORPHA:932Заболевание
Autosomal dominant, Autosomal recessive

Achondrogenesis type 1A

ORPHA:93299Клин. подт.
Autosomal recessive

Achondrogenesis type 1B

ORPHA:93298Клин. подт.
Autosomal recessive

Achondrogenesis type 2

ORPHA:93296Клин. подт.
Autosomal dominant

Achondroplasia

ORPHA:15Заболевание
Autosomal dominant

Achromatopsia

ORPHA:49382Заболевание
Autosomal recessive

Acinar cell carcinoma of pancreas

ORPHA:424046Заболевание
Not applicable

Acinar cystic transformation of the pancreas

ORPHA:695131Заболевание
Not applicable

Acitretin/etretinate embryopathy

ORPHA:40366Порок
Not applicable

Acquired Creutzfeldt-Jakob disease

ORPHA:454700Клин. гр.
Not applicable

Acquired aneurysmal subarachnoid hemorrhage

ORPHA:90065Ситуация
Not applicable

Acquired angioedema

ORPHA:91385Клин. гр.
Not applicable

Acquired angioedema type 1

ORPHA:100056Клин. подт.
Not applicable

Acquired angioedema type 2

ORPHA:100055Клин. подт.
Not applicable

Acquired angioedema with C1Inh deficiency

ORPHA:528663Заболевание
Not applicable

Acquired arginine vasopressin deficiency

ORPHA:95626Клин. подт.

Acquired cutis laxa

ORPHA:228285Заболевание
Not applicable

Acquired cystic disease-associated renal cell carcinoma

ORPHA:404514Заболевание

Acquired elastotic haemangioma

ORPHA:675597Заболевание

Acquired factor V deficiency

ORPHA:599490Заболевание