View source for Template:Multiple abnormalities

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| name  = Multiple abnormalities
| title = [[Congenital abnormality]]{{·}} [[multiple abnormalities]] ([[ICD-10_Chapter_XVII:_Congenital_malformations%2C_deformations_and_chromosomal_abnormalities#.28Q80-Q89.29_Other|Q87]], [[List of ICD-9 codes 740-759: Congenital anomalies#Other|759.7]])
| titlestyle = background:Silver

| group1 = [[Craniofacial abnormality|Craniofacial]]
|  list1 = [[Acrocephalosyndactylia]] ([[Apert syndrome]]/[[Pfeiffer syndrome]], [[Saethre-Chotzen syndrome]], [[Carpenter syndrome]], [[Sakati-Nyhan-Tisdale syndrome]])<BR>

''other:'' [[Möbius syndrome]]{{·}} [[Goldenhar syndrome]]{{·}} [[Cyclopia]]

| group2 = [[Short stature]]
|  list2 = [[Aarskog-Scott syndrome]]{{·}} [[Cockayne syndrome]]{{·}} [[Cornelia de Lange Syndrome]]{{·}} [[Dubowitz syndrome]]{{·}} [[Noonan syndrome]]{{·}} [[Robinow syndrome]]{{·}} [[Silver–Russell syndrome]]{{·}} [[Seckel syndrome]]{{·}} [[Smith-Lemli-Opitz syndrome]]-[[Turner syndrome]]

| group3 = [[Congenital limb deformities|Limb]]s
|  list3 = [[Adducted thumb syndrome]]{{·}} [[Holt-Oram syndrome]]{{·}} [[Klippel-Trénaunay-Weber syndrome]]{{·}} [[Nail–patella syndrome]]{{·}} [[Rubinstein-Taybi syndrome]]<BR>

[[Gastrulation]]/[[mesoderm]]: [[Caudal regression syndrome]]{{·}}  ''[[ectromelia]]'' ([[Sirenomelia]]){{·}} [[VACTERL association]]

| group4 = [[Overgrowth syndrome|Overgrowth]]
|  list4 = [[Beckwith-Wiedemann syndrome]]{{·}} [[Sotos syndrome]]{{·}} [[Weaver syndrome]]

| group6 = Laurence-Moon-Bardet-Biedl 
|  list6 = [[Bardet–Biedl syndrome]]{{·}} [[Laurence–Moon syndrome|Laurence-Moon syndrome]]

| group7 = Combined/other,<BR>known locus
|  list7 = ''[[Chromosome 3 (human)|3]]'' ([[Zimmerman-Laband syndrome]]){{·}} ''[[Chromosome 4 (human)|4]]/[[Chromosome 13 (human)|13]]'' ([[Fraser syndrome]]){{·}} ''[[Chromosome 8 (human)|8]]'' ([[Branchio-oto-renal syndrome]]){{·}} ''[[Chromosome 12 (human)|12]]'' ([[Keutel syndrome]], [[Timothy syndrome]]){{·}} ''[[Chromosome 15 (human)|15]]'' ([[Marfan syndrome]]){{·}} ''[[Chromosome 19 (human)|19]]'' ([[Donohue syndrome]]) 

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<includeonly>[[Category:Congenital disorders]]</includeonly>
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