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