Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/8
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- Michels Caskey syndrome
- Michels syndrome
- Mickleson syndrome
- Micrencephaly corpus callosum agenesis
- Micrencephaly olivopontocerebellar hypoplasia
- Micro syndrome
- Microbrachycephaly ptosis cleft lip
- Microcephalic osteodysplastic primordial dwarfism
- Microcephalic primordial dwarfism Toriello type
- Microcephalic primordial dwarfism
- Microcephaly albinism digital anomalies syndrome
- Microcephaly autosomal dominant
- Microcephaly brachydactyly kyphoscoliosis
- Microcephaly brain defect spasticity hypernatremia
- Microcephaly cardiac defect lung malsegmentation
- Microcephaly cardiomyopathy
- Microcephaly cervical spine fusion anomalies
- Microcephaly chorioretinopathy recessive form
- Microcephaly cleft palate autosomal dominant
- Microcephaly deafness syndrome
- Microcephaly developmental delay pancytopenia
- Microcephaly facial clefting preaxial polydactyly
- Microcephaly glomerulonephritis Marfanoid habitus
- Microcephaly hiatus hernia nephrotic syndrome
- Microcephaly hypergonadotropic hypogonadism short stature
- Microcephaly immunodeficiency lymphoreticuloma
- Microcephaly intracranial calcification
- Microcephaly lymphoedema chorioretinal dysplasia
- Microcephaly lymphoedema syndrome
- Microcephaly mental retardation retinopathy
- Microcephaly mental retardation spasticity epilepsy
- Microcephaly mesobrachyphalangy tracheoesophageal fistula syndrome
- Microcephaly microcornea syndrome Seemanova type
- Microcephaly micropenis convulsions
- Microcephaly microphthalmos blindness
- Microcephaly nonsyndromal
- Microcephaly pontocerebellar hypoplasia dyskinesia
- Microcephaly seizures mental retardation heart disorders
- Microcephaly sparse hair mental retardation seizures
- Microcephaly syndactyly brachymesophalangy
- Microcephaly with chorioretinopathy, autosomal dominant form
- Microcephaly with normal intelligence, immunodeficiency
- Microcephaly with spastic quadriplegia
- Microcephaly, holoprosencephaly, and intrauterine growth retardation
- Microcephaly, primary autosomal recessive
- Microcornea corectopia macular hypoplasia
- Microcornea glaucoma absent frontal sinuses
- Microdontia hypodontia short stature
- Microgastria limb reduction defect
- Microgastria short stature diabetes
- Microinfarct
- Micromelic dwarfism Fryns type
- Micromelic dysplasia dislocation of radius
- Microphtalmos bilateral colobomatous orbital cyst
- Microphthalmia camptodactyly mental retardation
- Microphthalmia cataract
- Microphthalmia diaphragmatic hernia Fallot
- Microphthalmia mental deficiency
- Microphthalmia microtia fetal akinesia
- Microphthalmia, Lentz type
- Microphthalmos, microcornea, and sclerocornea
- Microsomia hemifacial radial defects
- Microspherophakia metaphyseal dysplasia
- Microvillus inclusion disease
- Miculicz syndrome
- MIDAS syndrome
- Midline cleft of lower lip
- Midline defects autosomal type
- Midline defects recessive type
- Midline developmental field defects
- Midline field defects
- Midline lethal granuloma
- Mietens syndrome
- Mievis Verellen Dumoulin syndrome
- Mikulicz' Disease
- Mikulicz syndrome
- Milner Khallouf Gibson syndrome
- MILS syndrome
- Minkowski-Chauffard disease
- Minoxidil antenatal infection
- Miosis, congenital
- Mirror hands feet nasal defects
- Mirror polydactyly segmentation and limbs defects
- Misophobia
- Mitochondrial cytopathy (generic term)
- Mitochondrial diseases of nuclear origin
- Mitochondrial diseases, clinically undefinite
- Mitochondrial encephalomyopathy aminoacidopathy
- Mitochondrial genetic disorders
- Mitochondrial myopathy lactic acidosis
- Mitochondrial myopathy-encephalopathy-lactic acidosis
- Mitochondrial PEPCK deficiency
- Mitral regurgitation deafness skeletal anomalies
- Mitral valve prolapse, familial, autosomal dominant
- Mitral valve prolapse, familial, X linked (Mitral valve prolapse exists as an article but may not include these distinctions) --Jacqui★ 13:36, 25 July 2006 (UTC)
- Miura syndrome
- Mixed sclerosing bone dystrophy
- MLS syndrome
- MMEP syndrome
- MMT syndrome
- MN1
- MNGIE syndrome
- Moebius axonal neuropathy hypogonadism
- Moerman Van den berghe Fryns syndrome
- Mohr syndrome
- Mohr-Tranebjaerg syndrome
- Mollica Pavone Antener syndrome
- Moloney syndrome
- Molybdenum cofactor deficiency
- Monilethrix
- Monoamine oxidase A deficiency
- Monodactyly tetramelic
- Mononen Karnes Senac syndrome
- Monosomy 8q12 21
- Monosomy 8q21 q22
- Monosomy X
- Montefiore syndrome
- Moore Federman syndrome
- Moore Smith Weaver syndrome
- Morel's ear
- Moreno Zachai Kaufman syndrome
- Morgani Turner Albright syndrome
- Morhosseini Holmes Walton syndrome
- Morillo Cucci Passarge syndrome
- Morphea Scleroderma
- Morphea, generalized
- Morrison Young syndrome
- Morse Rawnsley Sargent syndrome
- Motor neuro-ophthalmic disorders
- Motor neuropathy peripheral dysautonomia
- Motor neuropathy
- Motor sensory neuropathy type 1 aplasia cutis congenita
- Mounier-Kuhn syndrome
- Mount Reback syndrome
- Mousa Al din Al Nassar syndrome
- MPS III-A
- MPS III-B
- MPS III-C
- MPS III-D
- MPS VI
- MSBD syndrome
- MTHFR deficiency
- Mucha-Habermann disease
- Mucoepithelial dysplasia
- Mucolipidosis type 1
- Mucolipidosis type 3
- Mucolipidosis type 4
- Mucosulfatidosis
- Muenke Syndrome
- Mulibrey Nanism syndrome
- Muller Barth Menger syndrome
- Mullerian aplasia
- Mullerian derivatives lymphangiectasia polydactyly
- Mullerian derivatives, persistent
- Mullerian duct abnormalities galactosemia
- Mulliez Roux Loterman syndrome
- Multicentric osteolysis nephropathy
- Multicentric reticulohistiocytosis
- Multifocal heterotopia
- Multifocal motor neuropathy with conduction block
- Multinodular goiter cystic kidney polydactyly
- Multiple acyl-CoA deficiency
- Multiple carboxylase deficiency, biotin responsive
- Multiple carboxylase deficiency, late onset
- Multiple carboxylase deficiency, propionic acidemia
- Multiple congenital anomalies mental retardation, growth failure and cleft lip palate
- Multiple congenital contractures
- Multiple contracture syndrome Finnish type
- Multiple fibrofolliculoma familial
- Multiple joint dislocations metaphyseal dysplasia
- Multiple pterygium syndrome lethal type
- Multiple pterygium syndrome
- Multiple sclerosis ichthyosis factor VIII deficiency
- Multiple subcutaneous angiolipomas
- Multiple sulfatase deficiency
- Multiple synostoses syndrome 1
- Multiple vertebral anomalies unusual facies
- Muscle-eye-brain syndrome
- Muscular atrophy ataxia retinitis pigmentosa diabetes mellitus
- Muscular dystrophy congenital infantile cataract hypogonadism
- Muscular dystrophy congenital, merosin negative
- Muscular dystrophy facioscapulohumeral
- Muscular dystrophy Hutterite type
- Muscular dystrophy limb girdle type 2A, Erb type
- Muscular dystrophy limb-girdle autosomal dominant
- Muscular dystrophy limb-girdle type 2B, Myoshi type
- Muscular dystrophy limb-girdle with beta-sarcoglycan deficiency
- Muscular dystrophy limb-girdle with delta-sarcoglyan deficiency
- Muscular dystrophy white matter spongiosis
- Muscular dystrophy, congenital, merosin-positive
- Muscular fibrosis multifocal obstructed vessels
- Muscular phosphorylase kinase deficiency
- Mutations in estradiol receptor
- Myalgia eosinophilia associated with tryptophan
- Myasthenia, familial
- Mycobacterium avium complex infection
- Mycosis fungoides, familial
- Mycositis fungoides
- Myelinopathies
- Myelocerebellar disorder
- Myelofibrosis, idiopathic
- Myelofibrosis-osteosclerosis
- Myeloid splenomegaly
- Myhre Ruvalcaba Graham syndrome
- Myhre Ruvalcaba Kelley syndrome
- Myhre School syndrome
- Myhre syndrome
- Myocardium disorder
- Myoclonic dystonia
- Myoclonic progressive familial epilepsy
- Myoclonus ataxia
- Myoclonus cerebellar ataxia deafness
- Myoclonus epilepsy partial seizure
- Myoclonus epilepsy
- Myoclonus hereditary progressive distal muscular atrophy
- Myoclonus progressive epilepsy of Unverricht and Lundborg
- Myoclonus with epilepsy with ragged red fibers (mitochondria)
- Myofibrillar lysis
- Myofibroblastic tumors
- Myoglobinuria dominant form
- Myoglobinuria recurrent
- Myoneurogastrointestinal encephalopathy syndrome
- Myopathy and diabetes mellitus
- Myopathy cataract hypogonadism
- Myopathy congenital multicore with external ophthalmoplegia
- Myopathy growth and mental retardation hypospadias
- Myopathy Hutterite type
- Myopathy mitochondrial cataract
- Myopathy Moebius Robin syndrome
- Myopathy ophthalmoplegia hypoacousia areflexia
- Myopathy tubular aggregates
- Myopathy with lactic acidosis and sideroblastic anemia
- Myopathy with lysis of myofibrils
- Myopathy, desmin storage
- Myopathy, McArdle type
- Myopathy, myotubular
- Myopathy, X-linked, with excessive autophagy
- Myophosphorylase deficiency
- Myopia, infantile severe
- Myositis ossificans post-traumatic
- Myotonia atrophica
- Myotonia mental retardation skeletal anomalies
- Myxoid liposarcoma
- Myxoma-spotty pigmentation-endocrine overactivity
- Myxomatous peritonitis
- N acetyltransferase deficiency
- N syndrome
- N-acetyl glutamate synthetase deficiency
- N-acetyl-alpha-D-galactosaminidase
- N-acetyl-glucosamine-6-sulfate sulfatase deficiency
- NADH CoQ reductase, deficiency of
- NADH cytochrome B5 reductase deficiency
- Naegeli syndrome
- Naguib syndrome
- Nail-patella syndrome
- Nakajo Nishimura syndrome
- Nakajo syndrome
- Nakamura Osame syndrome
- NAME syndrome
- Nance-Horan syndrome
- Nanism due to growth hormone combined deficiency
- Nanism due to growth hormone isolated deficiency with X linked hypogammaglobulinemia
- Nanism due to growth hormone resistance
- Narrow oral fissure short stature cone shaped epiphyses
- Nasodigitoacoustic syndrome
- Nasopalpebral lipoma coloboma syndrome
- Nasopharyngeal carcinoma
- Nasopharyngeal teratoma Dandy Walker diaphragmatic hernia
- Natal teeth intestinal pseudoobstruction patent ductus
- Nathalie syndrome
- Native American myopathy
- Navajo poikiloderma
- Necrotizing encephalopathy, infantile subacute
- Negative rheumatoid factor polyarthritis
- Nemaline Myopathy, Amish Type
- Neonatal ovarian cyst
- Neopharmaphobia
- Nephroblastomatosis,fetal ascites,macrosomia and Wilm's tumor
- Nephrocalcinosis
- Nephrolithiasis type 2
- Nephronophthisis familial adult spastic quadriparesis
- Nephropathy deafness hyperparathyroidism
- Nephropathy familial with hyperuricemia
- Nephropathy, familial with gout
- Nephrosclerosis
- Nephrosis deafness urinary tract digital malformation
- Nephrosis neuronal dysmigration syndrome
- Nephrotic syndrome ocular anomalies
- Nephrotic syndrome, idiopathic, steroid-resistant
- Nerve sheath neoplasm
- Nesidioblastosis of pancreas
- Netherton syndrome ichthyosis
- Neu Laxova syndrome
- Neuhauser Daly Magnelli syndrome
- Neuhauser Eichner Opitz syndrome
- Neural crest tumor
- Neural tube defects X linked
- Neuraminidase beta-galactosidase deficiency
- Neurilemmomatosis
- Neuritis with brachial predilection
- Neuroaxonal dystrophy renal tubular acidosis
- Neuroaxonal dystrophy, late infantile
- Neurocutaneous melanosis
- Neuroectodermal endocrine syndrome
- Neuroectodermal tumors primitive
- Neuroendocrine cancer
- Neuroendocrine carcinoma of the cervix
- Neuroepithelioma
- Neurofaciodigitorenal syndrome
- Neurofibromatosis type 3
- Neurofibromatosis type 6
- Neurofibromatosis, familial intestinal
- Neurofibromatosis, Type IV, of Riccardi
- Neurofibromatosis-Noonan syndrome
- Neurofibrosarcoma
- Neurogenic hypertension
- Neuroma biliary tract
- Neuronal heterotopia
- Neuronal interstitial dysplasia
- Neuronal intestinal pseudoobstruction
- Neuronal intranuclear hyaline inclusion disease
- Neuronal intranuclear inclusion disease
- Neuropathy ataxia and retinis pigmentosa
- Neuropathy congenital sensory neurotrophic keratitis
- Neuropathy hereditary with liability to pressure palsies
- Neuropathy motor sensory type 2 deafness mental retardation
- Neuropathy sensory spastic paraplegia
- Neuropathy, hereditary motor and sensory, LOM type
- Neuropathy, hereditary sensory, type I
- Neuropathy, hereditary sensory, type II
- Neutral lipid storage myopathy
- Neutropenia intermittent
- Neutropenia monocytopenia deafness
- Neutropenia, severe chronic
- Nevi flammei, familial multiple
- Nevo syndrome
- Nevus of ota retinitis pigmentosa
- Nevus sebaceus of Jadassohn
- Nicolaides Baraitser syndrome
- Niemann-Pick disease type D
- Night blindness skeletal anomalies unusual facies
- Night blindness, congenital stationary
- Nivelon Nivelon Mabille syndrome
- Noble Bass Sherman syndrome
- Non functioning pancreatic endocrine tumor
- Nonallergic atopic dermatitis
- Noninsulin-dependent diabetes mellitus with deafness
- Non-lissencephalic cortical dysplasia
- Nonmedullary thyroid carcinoma, with cell oxyphilia
- Nonne-Milroy disease
- Nonsyndromic hereditary hearing impairment
- Noonan like syndrome
- Norman Roberts lissencephaly syndrome
- Normokalemic periodic paralysis
- Northern epilepsy
- Norum disease
- Nose polyposis, familial
- Nosocomephobia
- Notalgia paresthetica
- Nova syndrome
- Novak syndrome
- Nuchal bleb, familial
- O Doherty syndrome
- O Donnell Pappas syndrome
- Obesophobia
- Obstructive asymmetric septal hypertrophy
- Occlusive Infantile ateriopathy
- Occult spinal dysraphism
- Occupational Asthma - Chemicals
- Occupational Asthma - Metals
- Occupational Asthma - Plants
- Occupational Asthma - Wood dust
- Occupational Asthma-Drugs
- Ochronosis, hereditary
- Ocular coloboma-imperforate anus
- Ocular convergence spasm
- Ocular Histoplasmosis
- Ocular melanoma
- Oculo cerebral dysplasia
- Oculo cerebro acral syndrome
- Oculo cerebro osseous syndrome
- Oculo dento digital dysplasia
- Oculo digital syndrome
- Oculo facio cardio dental syndrome
- Oculo skeletal renal syndrome
- Oculo tricho anal syndrome
- Oculo tricho dysplasia
- Oculoauriculofrontonasal syndrome
- Oculoauriculovertebral dysplasia
- Oculocerebral hypopigmentation syndrome Cross type
- Oculocerebral hypopigmentation syndrome type Preus
- Oculocerebral syndrome with hypopigmentation
- Oculocerebrocutaneous syndrome
- Oculocutaneous albinism immunodeficiency
- Oculocutaneous albinism, tyrosinase negative
- Oculocutaneous tyrosinemia
- Oculodental syndrome Rutherfurd syndrome
- Oculodentodigital dysplasia dominant
- Oculodentodigital syndrome
- Oculo-dento-digital syndrome
- Oculodentoosseous dysplasia dominant
- Oculodentoosseous dysplasia recessive
- Oculodigitoesophagoduodenal syndrome
- Oculo-gastrointestinal muscular dystrophy
- Oculomaxillofacial dysostosis
- Oculomaxillofacial dysplasia with oblique facial clefts
- Oculomelic amyoplasia
- Oculopalatoskeletal syndrome
- Oculorenocerebellar syndrome
- Odonto onycho dysplasia with alopecia
- Odontomicronychial dysplasia
- Odontoonychodermal dysplasia
- Odontotrichomelic hypohidrotic dysplasia
- OFD syndrome type 8
- OFD syndrome type Figuera
- Ohaha syndrome
- Ohdo Madokoro Sonoda syndrome
- Okamuto Satomura syndrome
- Oligodactyly tetramelic postaxial
- Oligomeganephronic renal hypoplasia
- Oligomeganephrony
- Oligophernia
- Oliver McFarlane syndrome
- Oliver syndrome
- Olivopontocerebellar atrophy deafness
- Olivopontocerebellar atrophy type 1
- Olivopontocerebellar atrophy type 2
- Olivopontocerebellar atrophy type 3
- Ollier disease
- Olmsted syndrome
- Ombrophobia
- Omodysplasia type 1
- Omphalocele cleft palate syndrome lethal
- Omphalocele exstrophy imperforate anus
- Omphalomesenteric cyst
- Onat syndrome
- Oneirophobia
- Onychonychia hypoplastic distal phalanges
- Onychotrichodysplasia and neutropenia
- Ophthalmic icthyosis
- Ophthalmo acromelic syndrome
- Ophthalmomandibulomelic dysplasia
- Ophthalmophobia
- Ophthalmoplegia ataxia hypoacusis
- Ophthalmoplegia mental retardation lingua scrotalis
- Ophthalmoplegia myalgia tubular aggregates
- Opitz Mollica Sorge syndrome
- Opitz Reynolds Fitzgerald syndrome
- Opitz syndrome
- Opsismodysplasia
- Opthalmoplegia progressive external scoliosis
- Optic atrophy opthalmoplegia ptosis deafness myopia
- Optic atrophy polyneuropathy deafness
- Optic atrophy, autosomal dominant A redirect, but not yet covered in Optic atrophy
- Optic atrophy, idiopathic, autosomal recessive
- Optic nerve coloboma with renal disease
- Optic nerve disorder
- Optic nerve hypoplasia, familial bilateral
- Optic pathway glioma
- Opticoacoustic nerve atrophy dementia
- Oral facial digital syndrome type 3
- Oral facial digital syndrome type 4
- Oral facial digital syndrome
- Oral facial dyskinesia
- Oral lichenoid lesions
- Oral squamous cell carcinoma
- Oral submucous fibrosis
- Oral-facial cleft
- Oral-facial-digital syndrome, type IV
- Oral-facial-digital syndrome
- Oral-pharyngeal disorders
- Organic brain syndrome
- Organic mood syndrome
- Organic personality syndrome
- Ornithine aminotransferase deficiency
- Ornithine carbamoyl phosphate deficiency
- Ornithine transcarbamylase deficiency, hyperammonemia due to
- Ornithinemia
- Oro acral syndrome
- Orofaciodigital syndrome Gabrielli type
- Orofaciodigital syndrome Shashi type
- Orofaciodigital syndrome Thurston type
- Orofaciodigital syndrome type 2
- Orofaciodigital syndrome type1
- Orotic aciduria hereditary
- Orotic aciduria purines-pyrimidines
- Orotidylic decarboxylase deficiency
- Orstavik Lindemann Solberg syndrome
- Osebold Remondini syndrome
- Oslam syndrome
- Osmed Syndrome
- Ossicular Malformations, familial
- Osteoarthropathy of fingers familial
- Osteochondritis deformans juvenile
- Osteochondrodysplasia thrombocytopenia hydrocephalus
- Osteocraniostenosis
- Osteodysplasia familial Anderson type
- Osteodysplastic dwarfism Corsello type
- Osteoectasia familial
- Osteogenesis imperfecta congenita microcephaly and cataracts
- Osteogenesis imperfecta congenital joint contractures
- Osteogenesis imperfecta retinopathy
- Osteogenic sarcoma
- Osteoglophonic dwarfism
- Osteolysis hereditary multicentric
- Osteolysis syndrome recessive
- Osteopathia condensans disseminata with osteopoikilosis
- Osteopathia striata cranial sclerosis
- Osteopathia striata pigmentary dermopathy white forelock
- Osteopetrosis autosomal dominant type 1
- Osteopetrosis lethal
- Osteopetrosis renal tubular acidosis
- Osteopetrosis, malignant
- Osteopetrosis, mild autosomal recessive form
- Osteopoikilosis
- Osteoporosis macrocephaly mental retardation blindness
- Osteoporosis oculocutaneous hypopigmentation syndrome
- Osteoporosis pseudoglioma syndrome
- Osteosarcoma limb anomalies erythroid macrocytosis
- Osteosclerose type Stanescu
- Osteosclerosis abnormalities of nervous system and meninges
- Osteosclerosis autosomal dominant Worth type
- Ostertag type amyloidosis
- Ota Kawamura Ito syndrome
- Oto palato digital syndrome type I and II
- Otodental dysplasia
- Otofaciocervical syndrome
- Otoonychoperoneal syndrome
- Oto-Palatal-digital syndrome
- Otopalatodigital syndrome type 2
- Otosclerosis, familial
- Ouvrier Billson syndrome
- Ovarian carcinosarcoma
- Ovarian dwarfism as part of Turner Syndrome
- Ovarian dwarfism
- Ovarian insufficiency due to FSH resistance
- Ovarian remnant syndrome
- Overfolded helix
- Overgrowth radial ray defect arthrogryposis
- Overgrowth syndrome type Fryer
- Overhydrated hereditary stomatocytosis
- Oxalosis
