MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
727 Erkrankungen gefunden (Kl. subt.) Zurücksetzen

Male infertility due to large-headed multiflagellar polyploid spermatozoa

ORPHA:137893Kl. subt.
Autosomal recessive

Malignant atrophic papulosis

ORPHA:679Kl. subt.
Autosomal dominant

Mandibuloacral dysplasia with type A lipodystrophy

ORPHA:90153Kl. subt.
Autosomal recessive

Mandibuloacral dysplasia with type B lipodystrophy

ORPHA:90154Kl. subt.
Autosomal recessive

Marfan syndrome type 1

ORPHA:284963Kl. subt.
Autosomal dominant

Marfan syndrome type 2

ORPHA:284973Kl. subt.
Autosomal dominant

Mayer-Rokitansky-Küster-Hauser syndrome type 1

ORPHA:247775Kl. subt.
Autosomal dominant, Not applicable

Mayer-Rokitansky-Küster-Hauser syndrome type 2

ORPHA:2578Kl. subt.
Autosomal dominant, Not applicable

Metachromatic leukodystrophy, adult form

ORPHA:309271Kl. subt.
Autosomal recessive

Metachromatic leukodystrophy, juvenile form

ORPHA:309263Kl. subt.
Autosomal recessive

Metachromatic leukodystrophy, late infantile form

ORPHA:309256Kl. subt.
Autosomal recessive

Methylcobalamin deficiency type cblDv1

ORPHA:308380Kl. subt.
Autosomal recessive

Methylcobalamin deficiency type cblE

ORPHA:2169Kl. subt.
Autosomal recessive

Methylcobalamin deficiency type cblG

ORPHA:2170Kl. subt.
Autosomal recessive

Methylmalonic acidemia with homocystinuria type cblF

ORPHA:79284Kl. subt.
Autosomal recessive

Methylmalonic acidemia with homocystinuria, type cblC

ORPHA:79282Kl. subt.
Autosomal recessive

Methylmalonic acidemia with homocystinuria, type cblD

ORPHA:79283Kl. subt.
Autosomal recessive

Methylmalonic acidemia with homocystinuria, type cblJ

ORPHA:369955Kl. subt.
Autosomal recessive

Methylmalonic acidemia with homocystinuria, type cblX

ORPHA:369962Kl. subt.
X-linked recessive

Mevalonic aciduria

ORPHA:29Kl. subt.
Autosomal recessive

Microcephaly-micromelia syndrome

ORPHA:572768Kl. subt.
Autosomal recessive

Microcephaly-short stature-limb abnormalities syndrome

ORPHA:572773Kl. subt.
Autosomal recessive

Midline interhemispheric variant of holoprosencephaly

ORPHA:93926Kl. subt.
Multigenic/multifactorial, Not applicable

Mild Canavan disease

ORPHA:314918Kl. subt.
Autosomal recessive