MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
727 diseases matched (Clin. sub.) Reset

Male infertility due to large-headed multiflagellar polyploid spermatozoa

ORPHA:137893Clin. sub.
Autosomal recessive

Malignant atrophic papulosis

ORPHA:679Clin. sub.
Autosomal dominant

Mandibuloacral dysplasia with type A lipodystrophy

ORPHA:90153Clin. sub.
Autosomal recessive

Mandibuloacral dysplasia with type B lipodystrophy

ORPHA:90154Clin. sub.
Autosomal recessive

Marfan syndrome type 1

ORPHA:284963Clin. sub.
Autosomal dominant

Marfan syndrome type 2

ORPHA:284973Clin. sub.
Autosomal dominant

Mayer-Rokitansky-Küster-Hauser syndrome type 1

ORPHA:247775Clin. sub.
Autosomal dominant, Not applicable

Mayer-Rokitansky-Küster-Hauser syndrome type 2

ORPHA:2578Clin. sub.
Autosomal dominant, Not applicable

Metachromatic leukodystrophy, adult form

ORPHA:309271Clin. sub.
Autosomal recessive

Metachromatic leukodystrophy, juvenile form

ORPHA:309263Clin. sub.
Autosomal recessive

Metachromatic leukodystrophy, late infantile form

ORPHA:309256Clin. sub.
Autosomal recessive

Methylcobalamin deficiency type cblDv1

ORPHA:308380Clin. sub.
Autosomal recessive

Methylcobalamin deficiency type cblE

ORPHA:2169Clin. sub.
Autosomal recessive

Methylcobalamin deficiency type cblG

ORPHA:2170Clin. sub.
Autosomal recessive

Methylmalonic acidemia with homocystinuria type cblF

ORPHA:79284Clin. sub.
Autosomal recessive

Methylmalonic acidemia with homocystinuria, type cblC

ORPHA:79282Clin. sub.
Autosomal recessive

Methylmalonic acidemia with homocystinuria, type cblD

ORPHA:79283Clin. sub.
Autosomal recessive

Methylmalonic acidemia with homocystinuria, type cblJ

ORPHA:369955Clin. sub.
Autosomal recessive

Methylmalonic acidemia with homocystinuria, type cblX

ORPHA:369962Clin. sub.
X-linked recessive

Mevalonic aciduria

ORPHA:29Clin. sub.
Autosomal recessive

Microcephaly-micromelia syndrome

ORPHA:572768Clin. sub.
Autosomal recessive

Microcephaly-short stature-limb abnormalities syndrome

ORPHA:572773Clin. sub.
Autosomal recessive

Midline interhemispheric variant of holoprosencephaly

ORPHA:93926Clin. sub.
Multigenic/multifactorial, Not applicable

Mild Canavan disease

ORPHA:314918Clin. sub.
Autosomal recessive