MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Acquired factor VII deficiency

ORPHA:599495Заболевание

Acquired factor X deficiency

ORPHA:599501Заболевание

Acquired factor XI deficiency

ORPHA:599507Заболевание

Acquired factor XIII deficiency

ORPHA:599513Заболевание

Acquired generalized lipodystrophy

ORPHA:79086Заболевание
Not applicable

Acquired hemophagocytic lymphohistiocytosis associated with malignant disease

ORPHA:158057Особая клин. ситуация

Acquired hemophilia A

ORPHA:599480Заболевание
Not applicable

Acquired hemophilia B

ORPHA:599485Заболевание
Not applicable

Acquired hypertrichosis lanuginosa

ORPHA:2221Заболевание
Not applicable

Acquired hypothalamic obesity

ORPHA:689401Заболевание
Not applicable

Acquired ichthyosis

ORPHA:454Заболевание
Not applicable

Acquired idiopathic sideroblastic anemia

ORPHA:75564Заболевание
Not applicable

Acquired intracranial dural arteriovenous fistula

ORPHA:715318Заболевание
Not applicable

Acquired methemoglobinemia

ORPHA:464453Заболевание
Not applicable

Acquired monoclonal Ig light chain-associated Fanconi syndrome

ORPHA:91136Заболевание
Not applicable

Acquired partial lipodystrophy

ORPHA:79087Заболевание
Multigenic/multifactorial, Not applicable

Acquired pseudoxanthoma elasticum

ORPHA:228247Заболевание
Not applicable

Acquired purpura fulminans

ORPHA:49566Заболевание
Not applicable

Acquired schizencephaly

ORPHA:485275Этиол. подтип

Acquired secondary polycythemia

ORPHA:238547Категория
Not applicable

Acquired von Willebrand syndrome

ORPHA:99147Заболевание
Not applicable

Acral peeling skin syndrome

ORPHA:263534Заболевание
Autosomal recessive

Acral persistent papular mucinosis

ORPHA:90396Заболевание

Acral self-healing collodion baby

ORPHA:281127Заболевание
Autosomal recessive, Unknown