Atlas Médico

Accessible medical knowledge

All Diseases

Multiminicore myopathy

Multinodular and vacuolating neuronal tumor

Multinodular goiter

Multinodular goiter-cystic kidney-polydactyly syndrome

Multiple acyl-CoA dehydrogenase deficiency

Multiple carboxylase deficiency

Multiple congenital anomalies due to 14q32.2 imprinting defect

Multiple congenital anomalies due to 14q32.2 maternally expressed gene defect

Multiple congenital anomalies due to 14q32.2 paternally expressed gene defect

Multiple congenital anomalies-hypotonia-seizures syndrome 1

Multiple congenital anomalies-hypotonia-seizures syndrome 2

Multiple congenital anomalies-hypotonia-seizures syndrome 3

Multiple cutaneous and mucosal venous malformations

Multiple endocrine neoplasia

Multiple endocrine neoplasia type 1

Multiple endocrine neoplasia type 2

Multiple endocrine neoplasia type 2A

Multiple endocrine neoplasia type 2B

Multiple endocrine neoplasia type 4

Multiple epiphyseal dysplasia

Multiple epiphyseal dysplasia due to collagen 9 anomaly

Multiple epiphyseal dysplasia type 1

Multiple epiphyseal dysplasia type 4

Multiple epiphyseal dysplasia type 5

Multiple epiphyseal dysplasia, Al-Gazali type

Multiple epiphyseal dysplasia, Beighton type

Multiple epiphyseal dysplasia, Lowry type

Multiple epiphyseal dysplasia, with miniepiphyses

Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia

Multiple fibroadenoma of the breast

Multiple intestinal atresia

Multiple mitochondrial dysfunctions syndrome 1

Multiple mitochondrial dysfunctions syndrome 2

Multiple mitochondrial dysfunctions syndrome 3

Multiple mitochondrial dysfunctions syndrome 4

Multiple mitochondrial dysfunctions syndrome 7

Multiple mitochondrial dysfunctions syndrome 9b

Multiple myeloma

Neoplasms

Multiple organ dysfunction syndrome

Multiple paragangliomas associated with polycythemia

Multiple personality disorder

Multiple pterygium-malignant hyperthermia syndrome

Multiple sclerosis

Neurological

Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome

Multiple self-healing squamous epithelioma

Multiple skull base meningioma

Multiple spinal canal and spinal cord meningioma

Multiple symmetric lipomatosis

Multiple symmetric lipomatosis with partial lipodystrophy

Multiple synostoses syndrome

Multiple synostoses syndrome 1

Multiple synostoses syndrome 2

Multiple synostoses syndrome 3

Multiple system atrophy

Multiple system atrophy, cerebellar type

Multiple system atrophy, parkinsonian type

Multisystem autoimmune disease due to IKAROS gain of function

Multisystemic smooth muscle dysfunction syndrome

Mumps infectious disease

Munchausen by proxy

Murray valley encephalitis

Muscle cancer

Muscle dysmorphic disorder

Muscle tissue disorder

Muscle-eye-brain disease

Muscle-eye-brain disease with bilateral multicystic leucodystrophy

Muscle-specific tyrosine kinase-associated myasthenia gravis

Muscular atrophy

Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome

Muscular channelopathy

Muscular dystrophy

Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10

Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11

Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12

Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4

Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7

Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8

Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1

Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2

Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3

Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6

Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2

Muscular dystrophy-dystroglycanopathy type B5

Muscular dystrophy-dystroglycanopathy type B6

Muscular dystrophy, limb-girdle, autosomal dominant

Muscular pseudohypertrophy-hypothyroidism syndrome

Musculoskeletal system benign neoplasm

Musculoskeletal system cancer

Musculoskeletal system disorder

Mushroom workers' lung

Mutism

Myalgia-eosinophilia syndrome associated with tryptophan

Myalgic encephalomeyelitis/chronic fatigue syndrome

Myasthenia gravis

Autoimmune

Myasthenic syndrome, congenital, 1B, fast-channel

MYCBP2-related developmental delay with corpus callosum defects

Mycetoma

Mycobacterial infectious disease

Mycobacterium avium complex disease

Mycobacterium xenopi infection