A–Z DIRECTORY
Conditions beginning with M
- Mabry syndromeAutosomal recessive
- MacrozoospermiaAutosomal recessive
- Maffucci syndromeNot inherited
- Mainzer-Saldino syndromeAutosomal recessive
- Majeed syndromeAutosomal recessive
- Mal de MeledaAutosomal recessive
- Malignant hyperthermiaAutosomal dominant
- Malonyl-CoA decarboxylase deficiencyAutosomal recessive
- Mandibuloacral dysplasiaAutosomal recessive
- Mandibulofacial dysostosis with microcephalyAutosomal dominant
- Manitoba oculotrichoanal syndromeAutosomal recessive
- Mannose-binding lectin deficiencyPattern unknown
- Maple syrup urine diseaseAutosomal recessive
- Marfan syndromeAutosomal dominant
- Marinesco-Sjögren syndromeAutosomal recessive
- Maternally inherited diabetes and deafnessMitochondrial
- Maturity-onset diabetes of the youngAutosomal dominant
- Mayer-Rokitansky-Küster-Hauser syndromePattern unknown · Autosomal dominant
- MBD5-associated neurodevelopmental disorderNot inherited · Autosomal dominant
- McCune-Albright syndromeNot inherited
- McKusick-Kaufman syndromeAutosomal recessive
- McLeod neuroacanthocytosis syndromeX-linked recessive
- MDA5 deficiencyAutosomal recessive · Autosomal dominant
- Meckel syndromeAutosomal recessive
- MECP2 duplication syndromeX-linked
- MECP2-related severe neonatal encephalopathyX-linked
- MED13L syndromeAutosomal dominant
- Medium-chain acyl-CoA dehydrogenase deficiencyAutosomal recessive
- Meesmann corneal dystrophyAutosomal dominant
- Megacystis-microcolon-intestinal hypoperistalsis syndromeAutosomal recessive · Autosomal dominant
- Megalencephalic leukoencephalopathy with subcortical cystsAutosomal recessive · Autosomal dominant
- Megalencephaly-capillary malformation syndromeNot inherited
- Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndromeAutosomal dominant
- MEGDEL syndromeAutosomal recessive
- Meier-Gorlin syndromeAutosomal recessive
- Meige diseaseAutosomal dominant
- MelanomaNot inherited · Autosomal dominant
- Melnick-Needles syndromeX-linked dominant
- MelorheostosisNot inherited
- Ménière diseaseAutosomal dominant
- Menkes syndromeX-linked recessive
- Metabolic dysfunction-associated steatotic liver diseasePattern unknown
- Metachromatic leukodystrophyAutosomal recessive
- Metatropic dysplasiaAutosomal dominant
- Methemoglobinemia, beta-globin typeAutosomal dominant
- Methylmalonic acidemiaAutosomal recessive
- Methylmalonic acidemia with homocystinuriaX-linked recessive · Autosomal recessive
- Mevalonate kinase deficiencyAutosomal recessive
- Microcephalic osteodysplastic primordial dwarfism type IIAutosomal recessive
- Microcephaly-capillary malformation syndromeAutosomal recessive
- Microcephaly, seizures, and developmental delayAutosomal recessive
- Microphthalmia with linear skin defects syndromeX-linked dominant
- Microvillus inclusion diseaseAutosomal recessive
- MigrainePattern unknown
- Miller syndromeAutosomal recessive
- Miller-Dieker syndromeNot inherited · Autosomal dominant
- Milroy diseaseAutosomal dominant
- Mitochondrial complex I deficiencyX-linked · Mitochondrial · Autosomal recessive
- Mitochondrial complex III deficiencyAutosomal recessive · Mitochondrial
- Mitochondrial complex V deficiencyAutosomal recessive · Mitochondrial
- Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodesMitochondrial
- Mitochondrial membrane protein-associated neurodegenerationAutosomal recessive
- Mitochondrial neurogastrointestinal encephalopathy diseaseAutosomal recessive
- Mitochondrial trifunctional protein deficiencyAutosomal recessive
- Miyoshi myopathyAutosomal recessive
- MN1 C-terminal truncation syndrome
- Moebius syndromePattern unknown
- Molybdenum cofactor deficiencyAutosomal recessive
- MonilethrixAutosomal recessive · Autosomal dominant
- Monoamine oxidase A deficiencyX-linked recessive
- Mosaic variegated aneuploidy syndromeAutosomal recessive
- Motion sicknessPattern unknown
- Mowat-Wilson syndromeAutosomal dominant
- Moyamoya diseaseAutosomal dominant · Pattern unknown
- MPV17-related hepatocerebral mitochondrial DNA depletion syndromeAutosomal recessive
- Mucolipidosis II alpha/betaAutosomal recessive
- Mucolipidosis III alpha/betaAutosomal recessive
- Mucolipidosis III gammaAutosomal recessive
- Mucolipidosis type IVAutosomal recessive
- Mucopolysaccharidosis type IAutosomal recessive
- Mucopolysaccharidosis type IIX-linked recessive
- Mucopolysaccharidosis type IIIAutosomal recessive
- Mucopolysaccharidosis type IVAutosomal recessive
- Mucopolysaccharidosis type VIAutosomal recessive
- Mucopolysaccharidosis type VIIAutosomal recessive
- Muenke syndromeAutosomal dominant
- Müllerian aplasia and hyperandrogenismAutosomal dominant
- Multicentric osteolysis, nodulosis, and arthropathyAutosomal recessive
- Multiminicore diseaseAutosomal recessive
- Multiple cutaneous and mucosal venous malformationsAutosomal dominant
- Multiple endocrine neoplasiaAutosomal dominant
- Multiple epiphyseal dysplasiaAutosomal dominant · Autosomal recessive
- Multiple familial trichoepitheliomaAutosomal dominant
- Multiple mitochondrial dysfunctions syndromeAutosomal recessive
- Multiple myelomaNot inherited · Pattern unknown
- Multiple pterygium syndromeAutosomal recessive
- Multiple sclerosisPattern unknown
- Multiple sulfatase deficiencyAutosomal recessive
- Multiple system atrophyPattern unknown
- MUTYH-associated polyposisAutosomal recessive
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