MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Didymosis aplasticosebacea

ORPHA:370046Заболевание
Not applicable

Diencephalic syndrome

ORPHA:1672Заболевание
Not applicable

Diencephalic-mesencephalic junction dysplasia

ORPHA:319192Морф. аномалия
Autosomal recessive

Dietary iron overload disease

ORPHA:139507Заболевание
Not applicable

Diethylstilbestrol syndrome

ORPHA:1916Мальформация
Not applicable

Difference of sex development-intellectual disability syndrome

ORPHA:2983Заболевание
Unknown

Differentiated thyroid carcinoma

ORPHA:146Заболевание
Not applicable

Diffuse alveolar hemorrhage

ORPHA:90060Clinical syndrome
Not applicable

Diffuse astrocytoma

ORPHA:251595Заболевание

Diffuse capillary malformation with overgrowth

ORPHA:714737Морф. аномалия
Not applicable

Diffuse cerebral and cerebellar atrophy-intractable seizures-progressive microcephaly syndrome

ORPHA:404437Мальформация
Autosomal recessive

Diffuse cutaneous mastocytosis

ORPHA:79456Заболевание
Not applicable

Diffuse cutaneous systemic sclerosis

ORPHA:220393Клин. подтип
Multigenic/multifactorial, Not applicable

Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia

ORPHA:617916Заболевание

Diffuse intrinsic pontine glioma

ORPHA:497188Заболевание

Diffuse large B-cell lymphoma

ORPHA:544Клин. группа
Multigenic/multifactorial, Not applicable

Diffuse large B-cell lymphoma of the central nervous system

ORPHA:300849Заболевание
Multigenic/multifactorial, Not applicable

Diffuse lymphatic malformation

ORPHA:141209Мальформация
Not applicable

Diffuse palmoplantar keratoderma with painful fissures

ORPHA:369999Заболевание
Autosomal dominant

Diffuse palmoplantar keratoderma, Bothnian type

ORPHA:2337Заболевание
Autosomal dominant

Diffuse palmoplantar keratoderma-acrocyanosis syndrome

ORPHA:86918Заболевание
Autosomal dominant

Diffuse panbronchiolitis

ORPHA:171700Заболевание
Multigenic/multifactorial

Digenic Alport syndrome

ORPHA:653722Клин. подтип
Autosomal dominant, Autosomal recessive

Digenic hemochromatosis

ORPHA:648581Заболевание