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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы
Найдено 727 заболеваний (Клин. подт.) Сброс

Male infertility due to large-headed multiflagellar polyploid spermatozoa

ORPHA:137893Клин. подт.
Autosomal recessive

Malignant atrophic papulosis

ORPHA:679Клин. подт.
Autosomal dominant

Mandibuloacral dysplasia with type A lipodystrophy

ORPHA:90153Клин. подт.
Autosomal recessive

Mandibuloacral dysplasia with type B lipodystrophy

ORPHA:90154Клин. подт.
Autosomal recessive

Marfan syndrome type 1

ORPHA:284963Клин. подт.
Autosomal dominant

Marfan syndrome type 2

ORPHA:284973Клин. подт.
Autosomal dominant

Mayer-Rokitansky-Küster-Hauser syndrome type 1

ORPHA:247775Клин. подт.
Autosomal dominant, Not applicable

Mayer-Rokitansky-Küster-Hauser syndrome type 2

ORPHA:2578Клин. подт.
Autosomal dominant, Not applicable

Metachromatic leukodystrophy, adult form

ORPHA:309271Клин. подт.
Autosomal recessive

Metachromatic leukodystrophy, juvenile form

ORPHA:309263Клин. подт.
Autosomal recessive

Metachromatic leukodystrophy, late infantile form

ORPHA:309256Клин. подт.
Autosomal recessive

Methylcobalamin deficiency type cblDv1

ORPHA:308380Клин. подт.
Autosomal recessive

Methylcobalamin deficiency type cblE

ORPHA:2169Клин. подт.
Autosomal recessive

Methylcobalamin deficiency type cblG

ORPHA:2170Клин. подт.
Autosomal recessive

Methylmalonic acidemia with homocystinuria type cblF

ORPHA:79284Клин. подт.
Autosomal recessive

Methylmalonic acidemia with homocystinuria, type cblC

ORPHA:79282Клин. подт.
Autosomal recessive

Methylmalonic acidemia with homocystinuria, type cblD

ORPHA:79283Клин. подт.
Autosomal recessive

Methylmalonic acidemia with homocystinuria, type cblJ

ORPHA:369955Клин. подт.
Autosomal recessive

Methylmalonic acidemia with homocystinuria, type cblX

ORPHA:369962Клин. подт.
X-linked recessive

Mevalonic aciduria

ORPHA:29Клин. подт.
Autosomal recessive

Microcephaly-micromelia syndrome

ORPHA:572768Клин. подт.
Autosomal recessive

Microcephaly-short stature-limb abnormalities syndrome

ORPHA:572773Клин. подт.
Autosomal recessive

Midline interhemispheric variant of holoprosencephaly

ORPHA:93926Клин. подт.
Multigenic/multifactorial, Not applicable

Mild Canavan disease

ORPHA:314918Клин. подт.
Autosomal recessive