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Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/8

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  1. Microbrachycephaly ptosis cleft lip
  2. Microcephaly hypergonadotropic hypogonadism short stature
  3. Microcephaly mental retardation retinopathy
  4. Microcephaly mental retardation spasticity epilepsy
  5. Microcephaly microcornea syndrome Seemanova type
  6. Microcephaly micropenis convulsions
  7. Microcephaly seizures mental retardation heart disorders
  8. Microcephaly, holoprosencephaly, and intrauterine growth retardation
  9. Microcornea corectopia macular hypoplasia
  10. Microdontia hypodontia short stature
  11. Microgastria limb reduction defect
  12. Microgastria short stature diabetes
  13. Micromelic dysplasia dislocation of radius
  14. Microsomia hemifacial radial defects
  15. Midline defects autosomal type
  16. Midline defects recessive type
  17. Midline developmental field defects
  18. Midline field defects
  19. Mievis Verellen Dumoulin syndrome
  20. Milner Khallouf Gibson syndrome
  21. Minoxidil antenatal infection
  22. Mirror hands feet nasal defects
  23. Mitochondrial PEPCK deficiency
  24. Miura syndrome
  25. Mixed sclerosing bone dystrophy
  26. Moebius axonal neuropathy hypogonadism
  27. Moisture-associated skin damage (MASD). "The four specific types of moisture-associated skin damage that will be discussed here are periwound moisture-associated dermatitis, peristomal moisture-associated dermatitis, incontinence-associated dermatitis, and intertriginous dermatitis."https://www.woundsource.com/patientcondition/moisture-associated-skin-damage-masd
  28. Mollica Pavone Antener syndrome
  29. Monodactyly tetramelic
  30. Mononen Karnes Senac syndrome
  31. Monosomy 8q12 21
  32. Monosomy 8q21 q22
  33. Montefiore syndrome
  34. Moore Smith Weaver syndrome
  35. Morgani Turner Albright syndrome
  36. Morillo Cucci Passarge syndrome
  37. Morrison Young syndrome
  38. Motor neuro-ophthalmic disorders
  39. Motor neuropathy peripheral dysautonomia
  40. MSBD syndrome
  41. Muller Barth Menger syndrome
  42. Mullerian derivatives lymphangiectasia polydactyly
  43. Mulliez Roux Loterman syndrome
  44. Multifocal heterotopia
  45. Multinodular goiter cystic kidney polydactyly
  46. Multiple congenital anomalies mental retardation, growth failure and cleft lip palate
  47. Multiple joint dislocations metaphyseal dysplasia
  48. Multiple pterygium syndrome lethal type
  49. Multiple synostoses syndrome 1
  50. Multiple vertebral anomalies unusual facies
  51. Muscular fibrosis multifocal obstructed vessels
  52. Myelofibrosis-osteosclerosis
  53. Myeloid splenomegaly
  54. Myhre Ruvalcaba Kelley syndrome
  55. Myhre School syndrome
  56. Myoclonus ataxia
  57. Myoclonus cerebellar ataxia deafness
  58. Myofibrillar lysis
  59. Myopathy cataract hypogonadism
  60. Myopathy growth and mental retardation hypospadias
  61. Myopathy ophthalmoplegia hypoacousia areflexia
  62. Myopathy with lysis of myofibrils
  63. Myotonia mental retardation skeletal anomalies
  64. N syndrome
  65. N-acetyl-alpha-D-galactosaminidase
  66. NADH CoQ reductase, deficiency of
  67. NADH cytochrome B5 reductase deficiency
  68. Narrow oral fissure short stature cone shaped epiphyses
  69. Nasopalpebral lipoma coloboma syndrome
  70. Nasopharyngeal teratoma Dandy Walker diaphragmatic hernia
  71. Natal teeth intestinal pseudoobstruction patent ductus
  72. Nephronophthisis familial adult spastic quadriparesis
  73. Nephropathy deafness hyperparathyroidism
  74. Nephropathy familial with hyperuricemia
  75. Nephropathy, familial with gout
  76. Nephrosis deafness urinary tract digital malformation
  77. Nephrotic syndrome ocular anomalies
  78. Neuhauser Daly Magnelli syndrome
  79. Neuhauser Eichner Opitz syndrome
  80. Neural crest tumor
  81. Neurofaciodigitorenal syndrome
  82. Neuronal intranuclear hyaline inclusion disease
  83. Neuronal intranuclear inclusion disease
  84. Neutropenia monocytopenia deafness
  85. Nevus of ota retinitis pigmentosa
  86. Night blindness skeletal anomalies unusual facies
  87. Nivelon Nivelon Mabille syndrome
  88. Noble Bass Sherman syndrome
  89. Nonmedullary thyroid carcinoma, with cell oxyphilia
  90. Noonan like syndrome
  91. Nova syndrome
  92. Novak syndrome
  93. O Doherty syndrome
  94. Ocular convergence spasm
  95. Oculo cerebro acral syndrome
  96. Oculo cerebro osseous syndrome
  97. Oculo digital syndrome
  98. Oculo skeletal renal syndrome
  99. Oculo tricho anal syndrome
  100. Oculo tricho dysplasia
  101. Oculocerebral hypopigmentation syndrome type Preus
  102. Oculodental syndrome Rutherfurd syndrome
  103. Oculo-gastrointestinal muscular dystrophy
  104. Oculomaxillofacial dysostosis
  105. Oculomaxillofacial dysplasia with oblique facial clefts
  106. Oculorenocerebellar syndrome
  107. Odonto onycho dysplasia with alopecia
  108. Odontomicronychial dysplasia
  109. Odontotrichomelic hypohidrotic dysplasia
  110. OFD syndrome type 8
  111. OFD syndrome type Figuera
  112. Oligodactyly tetramelic postaxial
  113. Omodysplasia type 1
  114. Omphalocele cleft palate syndrome lethal
  115. Omphalomesenteric cyst
  116. Onat syndrome
  117. Ophthalmomandibulomelic dysplasia
  118. Ophthalmoplegia mental retardation lingua scrotalis
  119. Opitz Mollica Sorge syndrome
  120. Opitz Reynolds Fitzgerald syndrome
  121. Oral facial digital syndrome type 4
  122. Oral-facial-digital syndrome, type IV
  123. Oro acral syndrome
  124. Orofaciodigital syndrome Gabrielli type
  125. Orofaciodigital syndrome Shashi type
  126. Orofaciodigital syndrome Thurston type
  127. Orofaciodigital syndrome type 2
  128. Ossicular Malformations, familial
  129. Osteoarthropathy of fingers familial
  130. Osteochondrodysplasia thrombocytopenia hydrocephalus
  131. Osteocraniostenosis
  132. Osteodysplastic dwarfism Corsello type
  133. Osteolysis syndrome recessive
  134. Osteopathia striata pigmentary dermopathy white forelock
  135. Osteoporosis macrocephaly mental retardation blindness
  136. Osteoporosis oculocutaneous hypopigmentation syndrome
  137. Osteosarcopenia (combined bone & muscle decline in aged)
  138. Otoonychoperoneal syndrome
  139. Ouvrier Billson syndrome
  140. Ovarian dwarfism
  141. Overfolded helix
  142. Overgrowth radial ray defect arthrogryposis