MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Multiple epiphyseal dysplasia type 7

ORPHA:647676Заболевание

Multiple epiphyseal dysplasia, Lowry type

ORPHA:166016Заболевание

Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome

ORPHA:166024Заболевание
Autosomal recessive

Multiple epiphyseal dysplasia-miniepiphyses syndrome

ORPHA:166032Заболевание

Multiple epiphyseal dysplasia-severe proximal femoral dysplasia syndrome

ORPHA:166029Заболевание

Multiple mitochondrial dysfunctions syndrome

ORPHA:289573Клин. группа
Autosomal recessive

Multiple mitochondrial dysfunctions syndrome type 1

ORPHA:401869Заболевание
Autosomal recessive

Multiple mitochondrial dysfunctions syndrome type 2

ORPHA:401874Заболевание
Autosomal recessive

Multiple mitochondrial dysfunctions syndrome type 3

ORPHA:363424Заболевание
Autosomal recessive

Multiple mitochondrial dysfunctions syndrome type 4

ORPHA:457406Заболевание
Autosomal recessive

Multiple mitochondrial dysfunctions syndrome type 5

ORPHA:569274Заболевание
Autosomal recessive

Multiple mitochondrial dysfunctions syndrome type 6

ORPHA:569290Заболевание
Autosomal recessive

Multiple myeloma

ORPHA:29073Заболевание
Not applicable

Multiple osteochondromas

ORPHA:321Заболевание
Autosomal dominant

Multiple paragangliomas associated with polycythemia

ORPHA:324299Заболевание
Not applicable

Multiple pterygium-malignant hyperthermia syndrome

ORPHA:2215Мальформация
Autosomal recessive

Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome

ORPHA:3151Заболевание
Unknown

Multiple self-healing squamous epithelioma

ORPHA:65748Заболевание
Autosomal dominant

Multiple sulfatase deficiency

ORPHA:585Заболевание
Autosomal recessive

Multiple symmetric lipomatosis

ORPHA:2398Заболевание
Autosomal dominant, Autosomal recessive, Mitochondrial inheritance, Not applicable

Multiple synostoses syndrome

ORPHA:3237Мальформация
Autosomal dominant

Multiple system atrophy

ORPHA:102Заболевание
Multigenic/multifactorial, Not applicable

Multiple system atrophy, cerebellar type

ORPHA:227510Клин. подтип
Not applicable

Multiple system atrophy, parkinsonian type

ORPHA:98933Клин. подтип
Not applicable