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Show new changes starting from 12:39, 6 August 2020
   
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6 August 2020

N    11:25  Cutaneous mastocytoma‎ (diff | hist) . . (+3,954). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' Cutaneous local mastocytoma; Multiple mastocytoma; Solitary mastocytoma Cutaneous mastocytoma is a form of cutaneous mastocytosis (CM, see this term) g...") (Tag: 2017 source edit)
     10:49  Congenital thrombotic thrombocytopenic purpura‎ (diff | hist) . . (+4,552). . Deepika vegiraju (talk | contribs) (Tag: 2017 source edit)
     10:06  Congenital pulmonary lymphangiectasia‎ (diff | hist) . . (+6,045). . Deepika vegiraju (talk | contribs) (Tag: 2017 source edit)
     09:13  Congenital erythropoietic porphyria‎ (diff | hist) . . (+4,226). . Deepika vegiraju (talk | contribs) (Removed redirect to Gunther disease) (Tags: Removed redirect, 2017 source edit)
N    08:24  Congenital dyserythropoietic anemia type 3‎ (diff | hist) . . (+4,071). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' Dyserythropoietic anemia, congenital type 3; CDA III Congenital dyserythropoietic anemia type III (CDA III) is a rare form of CDA (see this term) character...") (Tag: 2017 source edit)
N    08:07  Congenital dyserythropoietic anemia type 2‎ (diff | hist) . . (+4,432). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' CDAN2; Anemia, dyserythropoietic, congenital type 2; CDA II; Dyserythropoietic anemia, HEMPAS type; HEMPAS anemia; Hereditary Erythroblastic Multinuclearity...") (Tag: 2017 source edit)
N    06:21  Category:Anemias‎ (diff | hist) . . (+137). . Automatic category creator (talk | contribs) (Created automatically by the AutoCreateCategoryPages extension.)
N    06:21  Congenital dyserythropoietic anemia type 1‎ (diff | hist) . . (+4,231). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' CDA I; Dyserythropoietic anemia, congenital type 1; Anemia, dyserythropoietic, congenital type 1; Type I congenital dyserythropoietic anemia Congenital dys...") (Tag: 2017 source edit)
N    02:25  Category:Pathology stubs‎ (diff | hist) . . (+153). . Automatic category creator (talk | contribs) (Created automatically by the AutoCreateCategoryPages extension.)
N    02:25  Category:Albumin disorders‎ (diff | hist) . . (+157). . Automatic category creator (talk | contribs) (Created automatically by the AutoCreateCategoryPages extension.)
N    02:25  Congenital analbuminemia‎ (diff | hist) . . (+3,696). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:'''Analbuminemia; ANALBA Congenital analbuminemia (CAA) is a rare disorder characterized by the absence or very low levels of human serum albumin (HSA). I...") (Tag: 2017 source edit)

5 August 2020

     14:17  (Deletion log). . [Delete page script‎ (32×)]
     
14:17 . . Delete page script (talk | contribs) deleted page SUCLA2-Related Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form with Methylmalonic Aciduria
     
14:17 . . Delete page script (talk | contribs) deleted page X-linked spondyloepimetaphyseal dysplasia with hypomyelinating leukodystrophy (SEMDHL)
     
14:17 . . Delete page script (talk | contribs) deleted page Retinitis pigmentosa and intellectual disability due to Xp11.3 microdeletion
     
14:17 . . Delete page script (talk | contribs) deleted page Spondyloepiphyseal dysplasia with congenital joint dyslocations, CHST3 type
     
14:17 . . Delete page script (talk | contribs) deleted page Minimal information about a high-throughput sequencing experiment (MINSEQE)
     
14:17 . . Delete page script (talk | contribs) deleted page Scheie syndrome (subtype) formerly known as Mucopolysaccharidosis type V)
     
14:17 . . Delete page script (talk | contribs) deleted page Retinitis pigmentosa and intellectual disability due to del(X)(p11.3)
     
14:17 . . Delete page script (talk | contribs) deleted page X-linked intellectual disability-retinitis pigmentosa syndrome
     
14:17 . . Delete page script (talk | contribs) deleted page Sutherland-Haan X-linked intellectual disability syndrome
     
14:17 . . Delete page script (talk | contribs) deleted page Minimum information about a microarray experiment (MIAME)
     
14:17 . . Delete page script (talk | contribs) deleted page X-linked intellectual disability due to PQBP1 mutations
     
14:17 . . Delete page script (talk | contribs) deleted page Tyrosine hydroxylase-deficient dopa-responsive dystonia
     
14:17 . . Delete page script (talk | contribs) deleted page X-linked intellectual disability with spastic diplegia
     
14:17 . . Delete page script (talk | contribs) deleted page Qualified nonprofit agency for other severely disabled
     
14:17 . . Delete page script (talk | contribs) deleted page Mw:Special:MyLanguage/Help:VisualEditor/User guide/en
     
14:17 . . Delete page script (talk | contribs) deleted page TRAPPC11-related limb-girdle muscular dystrophy R18
     
14:17 . . Delete page script (talk | contribs) deleted page National Developmental Disabilities Awareness Month
     
14:17 . . Delete page script (talk | contribs) deleted page Mw:Special:MyLanguage/Help:VisualEditor/User guide
     
14:17 . . Delete page script (talk | contribs) deleted page Titin-related limb-girdle muscular dystrophy R10
     
14:17 . . Delete page script (talk | contribs) deleted page Vitamin B12-unresponsive methylmalonic acidemia
     
14:17 . . Delete page script (talk | contribs) deleted page TNP03-related limb-girdle muscular dystrophy D2
     
14:17 . . Delete page script (talk | contribs) deleted page Theodore superior limbic keratoconjunctivitis
     
14:17 . . Delete page script (talk | contribs) deleted page Qualified United States joint venture person
     
14:17 . . Delete page script (talk | contribs) deleted page X-linked scapuloperoneal muscular dystrophy
     
14:17 . . Delete page script (talk | contribs) deleted page National Colorectal Cancer Awareness Month
     
14:17 . . Delete page script (talk | contribs) deleted page Joint United Nations Programme on HIV/AIDS
     
14:17 . . Delete page script (talk | contribs) deleted page Functional Genomics Data (FGED) Society
     
14:17 . . Delete page script (talk | contribs) deleted page Comparative genomic hybridization (CGH)
     
14:17 . . Delete page script (talk | contribs) deleted page Qualifying domestic helium transaction
     
14:17 . . Delete page script (talk | contribs) deleted page Qualified individual with a disability
     
14:17 . . Delete page script (talk | contribs) deleted page National Endometriosis Awareness Month
     
14:17 . . Delete page script (talk | contribs) deleted page MicroArray and Gene Expression (MAGE)
     14:05  Human sexuality‎ (diff | hist) . . (+8). . Prab (talk | contribs) (Tag: 2017 source edit)
N b  14:02  New wave‎ (diff | hist) . . (+204). . PageBot (talk | contribs)
N b  14:02  Naturism‎ (diff | hist) . . (+67). . PageBot (talk | contribs)
N b  14:02  Macabre‎ (diff | hist) . . (+63). . PageBot (talk | contribs)
N b  14:02  Gymnosophy‎ (diff | hist) . . (+120). . PageBot (talk | contribs)
N b  14:02  Dress code‎ (diff | hist) . . (+170). . PageBot (talk | contribs)