MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Alpha-mannosidosis, infantile form

ORPHA:309282Клин. подтип
Autosomal recessive

Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3

ORPHA:62Заболевание
Autosomal recessive

Alpha-thalassemia

ORPHA:846Клин. группа
Autosomal recessive

Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16

ORPHA:98791Мальформация
Not applicable, Unknown

Alpha-thalassemia-myelodysplastic syndrome

ORPHA:231401Заболевание
Not applicable

Alport syndrome

ORPHA:63Заболевание
Autosomal dominant, Autosomal recessive, X-linked dominant

Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome

ORPHA:86818Заболевание
X-linked recessive

Alström syndrome

ORPHA:64Заболевание
Autosomal recessive

Alternating hemiplegia of childhood

ORPHA:2131Заболевание
Autosomal dominant, Not applicable

Alveolar echinococcosis

ORPHA:284Заболевание
Not applicable

Alveolar rhabdomyosarcoma

ORPHA:99756Клин. подтип
Multigenic/multifactorial

Alveolar soft tissue sarcoma

ORPHA:163699Заболевание
Not applicable

Amaurosis-hypertrichosis syndrome

ORPHA:1021Заболевание
Autosomal recessive

Amelo-onycho-hypohidrotic syndrome

ORPHA:1028Мальформация

Ameloblastic carcinoma

ORPHA:314422Заболевание
Not applicable

Ameloblastoma

ORPHA:314419Заболевание
Not applicable

Amelocerebrohypohidrotic syndrome

ORPHA:1946Мальформация
Autosomal recessive

Amelogenesis imperfecta

ORPHA:88661Заболевание
Autosomal dominant, Autosomal recessive, X-linked dominant

American trypanosomiasis

ORPHA:3386Заболевание
Not applicable

Aminoacylase 1 deficiency

ORPHA:137754Заболевание
Autosomal recessive

Aminopterin/methotrexate embryofetopathy

ORPHA:1908Мальформация
Not applicable

Amish lethal microcephaly

ORPHA:99742Мальформация
Autosomal recessive

Amish nemaline myopathy

ORPHA:98902Заболевание
Autosomal recessive

Amniotic band syndrome

ORPHA:295000Мальформация