Conditions: M

• Mabry syndromeClinical Genetics
• Macrocephaly-developmental delay syndromeClinical Genetics
• Macrocephaly-intellectual disability-left ventricular non compaction syndromeClinical Genetics
• Macrophage activation syndromeRheumatology
• MacrozoospermiaClinical Genetics
• Macular corneal dystrophyOphthalmology
• Macular DegenerationOphthalmology
• Maffucci syndromeOrthopaedics
• Mainzer-Saldino syndromeClinical Genetics
• Majeed syndromeRheumatology
• Mal de débarquementENT
• Mal de MeledaDermatology
• MalakoplakiaGastroenterology
• MalariaInfectious Diseases
• Male Breast CancerOncology
• Male InfertilityReproductive Medicine
• Male infertility with azoospermia or oligozoospermia due to single gene mutationReproductive Medicine
• Male infertility with teratozoospermia due to single gene mutationReproductive Medicine
• Malignant hyperthermiaClinical Genetics
• MalnutritionGeneral Medicine
• Malonyl-CoA decarboxylase deficiencyMetabolic Medicine
• MALT lymphomaOncology
• MAN1B1-CDGMetabolic Medicine
• Mandibuloacral dysplasiaOrthopaedics
• Mandibulofacial dysostosis with microcephalyClinical Genetics
• Manitoba oculotrichoanal syndromeClinical Genetics
• Mannose-binding lectin deficiencyClinical Genetics
• Maple syrup urine diseaseMetabolic Medicine
• Marburg hemorrhagic feverInfectious Diseases
• Marfan SyndromeRheumatology
• Marinesco-Sjögren syndromeNeurology
• Marshall syndromeOrthopaedics
• Maternally inherited diabetes and deafnessDiabetology
• Maturity-onset diabetes of the youngEndocrinology
• Mayer-Rokitansky-Küster-Hauser syndromeClinical Genetics
• MBD5-associated neurodevelopmental disorderClinical Genetics
• McCune-Albright syndromeOrthopaedics
• McKusick-Kaufman syndromeClinical Genetics
• McLeod neuroacanthocytosis syndromeNeurology
• MDA5 deficiencyClinical Genetics
• MeaslesInfectious Diseases
• Meckel syndromeClinical Genetics
• Meconium aspiration syndromePulmonology
• MECP2 duplication syndromeClinical Genetics
• MECP2-related severe neonatal encephalopathyNeurology
• MED13L syndromeClinical Genetics
• Medium-chain acyl-CoA dehydrogenase deficiencyMetabolic Medicine
• Medullary cystic kidney disease type 1Nephrology
• MedulloblastomaOncology
• Meesmann corneal dystrophyOphthalmology
• Megacystis-microcolon-intestinal hypoperistalsis syndromeClinical Genetics
• Megalencephalic leukoencephalopathy with subcortical cystsNeurology
• Megalencephaly-capillary malformation syndromeClinical Genetics
• Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndromeNeurology
• Megalencephaly-severe kyphoscoliosis-overgrowth syndromeClinical Genetics
• MEGDEL syndromeMetabolic Medicine
• Meier-Gorlin syndromeClinical Genetics
• Meige diseaseClinical Genetics
• MelanomaOncology
• MelioidosisInfectious Diseases
• Melnick-Needles syndromeOrthopaedics
• MelorheostosisOrthopaedics
• MEND syndromeNeurology
• Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiencyAllergy and Immunology
• Meniere's DiseaseENT
• MeningitisInfectious Diseases
• Meningococcal DiseaseInfectious Diseases
• Menke-Hennekam syndromeClinical Genetics
• Menkes syndromeMetabolic Medicine
• Mercury poisoningEmergency Medicine
• MesotheliomaOncology
• Metabolic dysfunction-associated steatotic liver diseaseHepatology
• Metabolic SyndromeEndocrinology
• Metachromatic leukodystrophyNeurology
• Metaphyseal chondrodysplasia, Jansen typeOrthopaedics
• Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduriaOrthopaedics
• Metatropic dysplasiaOrthopaedics
• Methanol poisoningEmergency Medicine
• Methemoglobinemia, beta-globin typeClinical Genetics
• Methotrexate toxicityEmergency Medicine
• Methylmalonic acidemiaClinical Genetics
• Methylmalonic acidemia with homocystinuriaMetabolic Medicine
• Mevalonate kinase deficiencyMetabolic Medicine
• MGAT2-CDGMetabolic Medicine
• Microcephalic cortical malformations-short stature due to RTTN deficiencyNeurology
• Microcephalic osteodysplastic primordial dwarfism type IIOrthopaedics
• Microcephalic osteodysplastic primordial dwarfism types I and IIIOrthopaedics
• Microcephaly, seizures, and developmental delayNeurology
• Microcephaly-capillary malformation syndromeClinical Genetics
• Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromeClinical Genetics
• Microphthalmia with linear skin defects syndromeClinical Genetics
• Microphthalmia, Lenz typeClinical Genetics
• Microscopic polyangiitisRheumatology
• MicrosporidiosisInfectious Diseases
• Microvillus inclusion diseaseGastroenterology
• MigraineNeurology
• Mild Cognitive ImpairmentPsychiatry
• Miller syndromeClinical Genetics
• Miller-Dieker syndromeClinical Genetics
• Milroy diseaseClinical Genetics
• Mirizzi syndromeHepatology
• MiscarriageObstetrics and Gynaecology
• Mitochondrial complex I deficiencyClinical Genetics
• Mitochondrial complex III deficiencyClinical Genetics
• Mitochondrial complex V deficiencyClinical Genetics
• Mitochondrial DNA-associated Leigh syndromeMetabolic Medicine
• Mitochondrial DNA-related cardiomyopathy and hearing lossCardiology
• Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodesNeurology
• Mitochondrial membrane protein-associated neurodegenerationNeurology
• Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndromeClinical Genetics
• Mitochondrial neurogastrointestinal encephalopathy diseaseGastroenterology
• Mitochondrial trifunctional protein deficiencyMetabolic Medicine
• Mitral Valve ProlapseCardiology
• Mixed connective tissue diseaseRheumatology
• Mixed-type autoimmune hemolytic anemiaHaematology
• Miyoshi myopathyNeurology
• Moebius syndromeClinical Genetics
• MOGS-CDGMetabolic Medicine
• MolesDermatology
• Molybdenum cofactor deficiencyClinical Genetics
• MonilethrixDermatology
• Monoamine oxidase A deficiencyMetabolic Medicine
• Monosomy 13q14 syndromeClinical Genetics
• Mosaic variegated aneuploidy syndromeClinical Genetics
• Motion SicknessClinical Genetics
• Mounier-Kühn syndromePulmonology
• Mowat-Wilson syndromeClinical Genetics
• Moyamoya diseaseNeurology
• MpoxInfectious Diseases
• MPV17-related hepatocerebral mitochondrial DNA depletion syndromeClinical Genetics
• MRSAInfectious Diseases
• Muckle-Wells syndromeRheumatology
• Mucolipidosis II alpha/betaClinical Genetics
• Mucolipidosis III alpha/betaClinical Genetics
• Mucolipidosis III gammaClinical Genetics
• Mucolipidosis type IVMetabolic Medicine
• Mucopolysaccharidosis type IMetabolic Medicine
• Mucopolysaccharidosis type IIMetabolic Medicine
• Mucopolysaccharidosis type IIIMetabolic Medicine
• Mucopolysaccharidosis type IVMetabolic Medicine
• Mucopolysaccharidosis type VIMetabolic Medicine
• Mucopolysaccharidosis type VIIMetabolic Medicine
• Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disordersClinical Genetics
• Muenke syndromeClinical Genetics
• Multicentric osteolysis, nodulosis, and arthropathyClinical Genetics
• Multicentric osteolysis-nodulosis-arthropathy spectrumRheumatology
• Multifocal lymphangioendotheliomatosis-thrombocytopenia syndromeOncology
• Multiminicore diseaseNeurology
• Multiple benign circumferential skin creases on limbsDermatology
• Multiple congenital anomalies-hypotonia-seizures syndromeClinical Genetics
• Multiple cutaneous and mucosal venous malformationsClinical Genetics
• Multiple endocrine neoplasiaClinical Genetics
• Multiple endocrine neoplasia type 1Oncology
• Multiple endocrine neoplasia type 2Oncology
• Multiple endocrine neoplasia type 4Oncology
• Multiple epiphyseal dysplasiaClinical Genetics
• Multiple epiphyseal dysplasia due to collagen 9 anomalyOrthopaedics
• Multiple epiphyseal dysplasia type 4Orthopaedics
• Multiple epiphyseal dysplasia type 5Orthopaedics
• Multiple familial trichoepitheliomaClinical Genetics
• Multiple mitochondrial dysfunctions syndromeClinical Genetics
• Multiple mitochondrial dysfunctions syndrome type 1Metabolic Medicine
• Multiple mitochondrial dysfunctions syndrome type 2Metabolic Medicine
• Multiple mitochondrial dysfunctions syndrome type 3Neurology
• Multiple mitochondrial dysfunctions syndrome type 4Metabolic Medicine
• Multiple MyelomaOncology
• Multiple pterygium syndromeClinical Genetics
• Multiple SclerosisNeurology
• Multiple sulfatase deficiencyMetabolic Medicine
• Multiple system atrophyNeurology
• MumpsInfectious Diseases
• Muscle CrampsOrthopaedics
• Muscular DystrophyNeurology
• Musculocontractural Ehlers-Danlos syndromeRheumatology
• Mutilating palmoplantar keratoderma with periorificial keratotic plaquesDermatology
• MUTYH-associated polyposisClinical Genetics
• Myalgic Encephalomyelitis/Chronic Fatigue SyndromeNeurology
• Myasthenia GravisNeurology
• MycetomaInfectious Diseases
• Mycobacterial InfectionsInfectious Diseases
• Mycosis fungoidesClinical Genetics
• MyD88 deficiencyClinical Genetics
• Myelodysplastic neoplasm with increased blastsOncology
• Myelodysplastic neoplasm with low blastsOncology
• Myelodysplastic SyndromesHaematology
• MYH9-related disorderHaematology
• Myhre syndromeClinical Genetics
• Myoclonic epilepsy myopathy sensory ataxiaNeurology
• Myoclonic epilepsy with ragged-red fibersNeurology
• Myoclonus-dystoniaNeurology
• Myofibrillar myopathyClinical Genetics
• Myopathic Ehlers-Danlos syndromeRheumatology
• Myopathy with deficiency of iron-sulfur cluster assembly enzymeClinical Genetics
• Myosin storage myopathyNeurology
• MyositisNeurology
• Myostatin-related muscle hypertrophyClinical Genetics
• Myotonia congenitaNeurology
• Myotonic dystrophyClinical Genetics
• MYT1L-related developmental delay-intellectual disability-obesity syndromeNeurology
• Ménétrier diseaseGastroenterology
• Müllerian aplasia and hyperandrogenismClinical Genetics