Difference between revisions of "Template:Congenital malformations and deformations of integument"

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| groupstyle = background-color: Linen
 
| groupstyle = background-color: Linen
  
   | group1 = [[Congenital ichthyosis]]
+
   | group1 = [[Congenital ichthyosis]]/<BR>[[erythrokeratodermia]]
 
   |  list1 = {{Navbox subgroup
 
   |  list1 = {{Navbox subgroup
 
| groupstyle = background-color: Linen
 
| groupstyle = background-color: Linen
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}}
 
}}
  
   | group2 = [[Epidermolysis bullosa]]
+
   | group2 = [[Epidermolysis bullosa]]<BR>and related
 
   |  list2 = <div>[[Epidermolysis bullosa simplex]] ([[Generalized epidermolysis bullosa simplex|Generalized]], [[Localized epidermolysis bullosa simplex|Localized]], [[Epidermolysis bullosa herpetiformis|Herpetiformis]], [[Epidermolysis bullosa simplex of Ogna|Ogna]], [[Epidermolysis bullosa simplex with muscular dystrophy|With muscular dystrophy]], [[Epidermolysis bullosa simplex with mottled pigmentation|With mottled pigmentation]])</div>
 
   |  list2 = <div>[[Epidermolysis bullosa simplex]] ([[Generalized epidermolysis bullosa simplex|Generalized]], [[Localized epidermolysis bullosa simplex|Localized]], [[Epidermolysis bullosa herpetiformis|Herpetiformis]], [[Epidermolysis bullosa simplex of Ogna|Ogna]], [[Epidermolysis bullosa simplex with muscular dystrophy|With muscular dystrophy]], [[Epidermolysis bullosa simplex with mottled pigmentation|With mottled pigmentation]])</div>
 
<div>[[Junctional epidermolysis bullosa (medicine)|Junctional epidermolysis bullosa]] ([[Junctional epidermolysis bullosa gravis|Gravis]], [[Mitis junctional epidermolysis bullosa|Mitis]], [[Generalized atrophic benign epidermolysis bullosa|Generalized atrophic]], [[Cicatricial junctional epidermolysis bullosa|Cicatricial]], [[Junctional epidermolysis bullosa with pyloric atresia|With pyloric atresia]])</div>
 
<div>[[Junctional epidermolysis bullosa (medicine)|Junctional epidermolysis bullosa]] ([[Junctional epidermolysis bullosa gravis|Gravis]], [[Mitis junctional epidermolysis bullosa|Mitis]], [[Generalized atrophic benign epidermolysis bullosa|Generalized atrophic]], [[Cicatricial junctional epidermolysis bullosa|Cicatricial]], [[Junctional epidermolysis bullosa with pyloric atresia|With pyloric atresia]])</div>
 
<div>[[Epidermolysis bullosa dystrophica]] ([[Dominant dystrophic epidermolysis bullosa|Dominant]], [[Recessive dystrophic epidermolysis bullosa|Recessive]])</div>
 
<div>[[Epidermolysis bullosa dystrophica]] ([[Dominant dystrophic epidermolysis bullosa|Dominant]], [[Recessive dystrophic epidermolysis bullosa|Recessive]])</div>
 +
 +
related: [[Costello syndrome]]{{·}} [[Kindler syndrome]]{{·}} [[Laryngoonychocutaneous syndrome]]{{·}} [[Skin fragility syndrome]]{{·}}
 +
 
| group3 = [[Pigmentation disorder]]
 
| group3 = [[Pigmentation disorder]]
   |  list3 = [[Incontinentia pigmenti]] {{·}} [[Urticaria pigmentosa]]{{·}} [[Lelis syndrome]]
+
   |  list3 = ''see [[Template:Pigmentation disorders]]''
 +
 
 
| group4 = [[DNA repair-deficiency disorder]]
 
| group4 = [[DNA repair-deficiency disorder]]
   |  list4 = [[Bloom syndrome]]{{·}} [[Rothmund–Thomson syndrome]]{{·}} [[Xeroderma pigmentosum]]
+
   |  list4 = ''see [[Template:DNA replication and repair-deficiency disorder]]''
 +
 
 
| group5 = [[Ectodermal dysplasia]]
 
| group5 = [[Ectodermal dysplasia]]
   |  list5 = [[Naegeli syndrome]]/[[Dermatopathia pigmentosa reticularis]]{{·}} [[Hay–Wells syndrome]]{{·}} [[Hypohidrotic ectodermal dysplasia]]{{·}} [[Focal dermal hypoplasia]]{{·}} [[Ellis–van Creveld syndrome]]
+
   |  list5 = [[Naegeli syndrome]]/[[Dermatopathia pigmentosa reticularis]]{{·}} [[Hay–Wells syndrome]]{{·}} [[Hypohidrotic ectodermal dysplasia]]{{·}} [[Focal dermal hypoplasia]]{{·}} [[Ellis–van Creveld syndrome]]{{·}} [[Rapp–Hodgkin syndrome]]/[[Hay–Wells syndrome]]
 +
 
 +
| group6 = [[Elastic fiber|Elastic]]/[[Connective tissue disease|Connective]]
 +
  |  list6 = [[Ehlers–Danlos syndrome]]{{·}} [[Cutis laxa]] ([[Gerodermia osteodysplastica]]){{·}} [[Popliteal pterygium syndrome]]{{·}} [[Pseudoxanthoma elasticum]]{{·}} [[Van Der Woude syndrome]]
 +
 
 
| group7 = [[Hyperkeratosis]]/[[Keratin disease|keratinopathy]]
 
| group7 = [[Hyperkeratosis]]/[[Keratin disease|keratinopathy]]
 
   |  list7 = <div>[[Meleda disease]]{{·}} [[Keratosis pilaris]]{{·}} ''[[ATP2A2]]'' ([[Darier's disease]]){{·}} [[Dyskeratosis congenita]]{{·}} [[Lelis syndrome]]</div>
 
   |  list7 = <div>[[Meleda disease]]{{·}} [[Keratosis pilaris]]{{·}} ''[[ATP2A2]]'' ([[Darier's disease]]){{·}} [[Dyskeratosis congenita]]{{·}} [[Lelis syndrome]]</div>
 
<div>[[Dyskeratosis congenita]]{{·}} [[Keratolytic winter erythema]]{{·}} [[Keratosis follicularis spinulosa decalvans]]{{·}} [[Keratosis linearis with ichthyosis congenital and sclerosing keratoderma syndrome]]{{·}} [[Keratosis pilaris atrophicans faciei]]{{·}} [[Keratosis pilaris]]</div>
 
<div>[[Dyskeratosis congenita]]{{·}} [[Keratolytic winter erythema]]{{·}} [[Keratosis follicularis spinulosa decalvans]]{{·}} [[Keratosis linearis with ichthyosis congenital and sclerosing keratoderma syndrome]]{{·}} [[Keratosis pilaris atrophicans faciei]]{{·}} [[Keratosis pilaris]]</div>
 +
 +
''see also [[Template:Cutaneous keratosis, ulcer, atrophy, and necrobiosis]]''
 +
 
| group8 = [[Nevus]]
 
| group8 = [[Nevus]]
 
   |  list8 = [[Capillary hemangioma]]{{·}} [[Port-wine stain]] ([[Nevus flammeus nuchae]])
 
   |  list8 = [[Capillary hemangioma]]{{·}} [[Port-wine stain]] ([[Nevus flammeus nuchae]])
 
| group9 = Other
 
| group9 = Other
   |  list9 = [[Familial cutaneous papillomatosis]]{{·}} [[Kindler syndrome]]{{·}} ''[[cadherin]]'' ([[EEM syndrome]]){{·}} ''[[immune system]]'' ([[Lymphedema|Hereditary lymphedema]], [[Mastocytosis]]){{·}} [[Hailey–Hailey disease|Hailey–Hailey]]{{·}} [[Birthmark]]{{·}} [[Aplasia cutis congenita]]
+
   |  list9 = [[Familial cutaneous papillomatosis]]{{·}} ''[[cadherin]]'' ([[EEM syndrome]]){{·}} ''[[immune system]]'' ([[Lymphedema|Hereditary lymphedema]], [[Mastocytosis]]/[[Urticaria pigmentosa]]){{·}} [[Hailey–Hailey disease|Hailey–Hailey]]{{·}} [[Birthmark]]{{·}} [[Aplasia cutis congenita]]<BR>
 +
 
 +
''see also [[Template:Congenital malformations and deformations of skin appendages]], [[Template:Phakomatoses]]''
 
}}
 
}}
  
| group3 = [[Elastic fiber|Elastic]]/[[Connective tissue disease|Connective]]
 
|  list3 = [[Cutis laxa]] ([[Gerodermia osteodysplastica]]){{·}} [[Pseudoxanthoma elasticum]]
 
| group4 = Ungrouped cutaneous<br />congenital anomalies
 
| list4 = {{Navbox subgroup
 
| groupstyle =
 
| liststyle  =
 
  
| group1 = With OMIM
+
| group4 = Developmental<BR>[[anomalies]]
| list1  = [[Accessory tragus]]{{·}} [[Amniotic band syndrome]]{{·}} [[Aplasia cutis congenita]]{{·}} [[Branchial cyst]]{{·}} [[Cavernous venous malformation]]
+
| list4 = [[Accessory tragus]]{{·}} [[Amniotic band syndrome]]{{·}} [[Branchial cyst]]{{·}} [[Cavernous venous malformation]]<BR>
| group2 = Without OMIM
 
| list2  = [[Accessory nail of the fifth toe]]{{·}} [[Arteriovenous fistula]]{{·}} [[Bronchogenic cyst]]{{·}} [[Congenital cartilaginous rest of the neck]]{{·}} [[Congenital hypertrophy of the lateral fold of the hallux]]{{·}} [[Congenital lip pit]]{{·}} [[Congenital malformations of the dermatoglyphs]]{{·}} [[Congenital preauricular fistula]]{{·}} [[Congenital smooth muscle hamartoma]]{{·}} [[Cystic lymphatic malformation]]{{·}} [[Dermoid cyst]]{{·}} [[Encephalocele]]{{·}} [[Infantile hemangioma]]{{·}} [[Malignant pilomatricoma]]{{·}} [[Median raphe cyst]]{{·}} [[Melanotic neuroectodermal tumor of infancy]]{{·}} [[Mongolian spot]]{{·}} [[Nasal glioma]]{{·}} [[Nasolacrimal duct cyst]]{{·}} [[Omphalomesenteric duct cyst]]{{·}} [[Pilomatricoma]]{{·}} [[Poland anomaly]]{{·}} [[PHACE association]]{{·}} [[Rapidly involuting congenital hemangioma]]{{·}} [[Rosenthal–Kloepfer syndrome]]{{·}} [[Rudimentary supernumerary digit]]{{·}} [[Sinus pericranii]]{{·}} [[Skin dimple]]{{·}} [[Superficial lymphatic malformation]]{{·}} [[Supernumerary nipple]]{{·}} [[Thyroglossal duct cyst]]{{·}} [[Verrucous vascular malformation]]
 
}}
 
  
| group5 = Ungrouped<br />[[genodermatoses]]
+
[[Accessory nail of the fifth toe]]{{·}} [[Arteriovenous fistula]]{{·}} [[Bronchogenic cyst]]{{·}} [[Congenital cartilaginous rest of the neck]]{{·}} [[Congenital hypertrophy of the lateral fold of the hallux]]{{·}} [[Congenital lip pit]]{{·}} [[Congenital malformations of the dermatoglyphs]]{{·}} [[Congenital preauricular fistula]]{{·}} [[Congenital smooth muscle hamartoma]]{{·}} [[Cystic lymphatic malformation]]{{·}} [[Dermoid cyst]]{{·}} [[Encephalocele]]{{·}} [[Infantile hemangioma]]{{·}} [[Malignant pilomatricoma]]{{·}} [[Median raphe cyst]]{{·}} [[Melanotic neuroectodermal tumor of infancy]]{{·}} [[Mongolian spot]]{{·}} [[Nasal glioma]]{{·}} [[Nasolacrimal duct cyst]]{{·}} [[Omphalomesenteric duct cyst]]{{·}} [[Pilomatricoma]]{{·}} [[Poland anomaly]]{{·}} [[PHACE association]]{{·}} [[Rapidly involuting congenital hemangioma]]{{·}} [[Rosenthal–Kloepfer syndrome]]{{·}} [[Rudimentary supernumerary digit]]{{·}} [[Sinus pericranii]]{{·}} [[Skin dimple]]{{·}} [[Superficial lymphatic malformation]]{{·}} [[Supernumerary nipple]]{{·}} [[Thyroglossal duct cyst]]{{·}} [[Verrucous vascular malformation]]
| list5 = {{Navbox subgroup
 
| groupstyle =
 
| liststyle  =
 
  
| group1 = With OMIM
 
| list1  = <div>STRUCTURAL: ''cytoskeleton'' [[Gardner's syndrome]]{{·}} [[Skin fragility syndrome]]{{·}} [[Naegeli–Franceschetti–Jadassohn syndrome]]{{·}} [[Laryngoonychocutaneous syndrome]]{{·}} [[Freeman–Sheldon syndrome]]{{·}} [[Terminal osseous dysplasia with pigmentary defects]]{{·}} ''cilia'' [[Joubert syndrome]]{{·}} ''peroxisome'' [[Rhizomelic chondrodysplasia punctata]]{{·}} [[Refsum's disease]]{{·}} ''nucleus:'' [[Franceschetti–Klein syndrome]]{{·}} [[Schinzel–Giedion syndrome]]{{·}} [[Treacher Collins syndrome]]{{·}} ''ecm:'' [[Transient bullous dermolysis of the newborn]]{{·}} [[Bart syndrome]]</div>
 
<div>DNA/RNA/PROTEIN SYNTHESIS: ''transcription factor:'' [[Atrichia with papular lesions]]{{·}} [[Autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy syndrome]]{{·}} [[Tooth and nail syndrome]]{{·}} [[Kabuki syndrome]]{{·}} [[Rapp–Hodgkin syndrome]]/[[Hay–Wells syndrome]]{{·}} [[Ectrodactyly–ectodermal dysplasia–cleft syndrome]]{{·}} [[Ulnar–mammary syndrome]]{{·}} [[Popliteal pterygium syndrome]]{{·}} [[IPEX syndrome]]{{·}} [[Townes–Brocks syndrome]]{{·}} [[Tricho–rhino–phalangeal syndrome]]{{·}} [[Van Der Woude syndrome]]{{·}} ''repair:'' [[Bloom syndrome]]{{·}} [[Cockayne syndrome]]{{·}} [[DeSanctis–Cacchione syndrome]]{{·}} [[Werner syndrome]]{{·}} [[IBIDS syndrome]]{{·}} [[Rothmund–Thomson syndrome]]{{·}} ''postranslational:'' [[Johanson–Blizzard syndrome]]{{·}} ''ribonucleoprotein:'' [[Cartilage–hair hypoplasia]]</div>
 
<div>MEMBRANE: ''membrane transport protein:'' [[Acrodermatitis enteropathica]]{{·}} [[Oculodentodigital dysplasia]]{{·}} ''ion pump disorders:'' [[Acrokeratosis verruciformis]]{{·}} [[Progressive symmetric erythrokeratodermia]]{{·}} [[Hallerman–Streiff syndrome]]{{·}} ''other:'' [[Kindler syndrome]]</div>
 
<div>TRANSDUCTION: ''receptor:'' [[Apert syndrome]]{{·}} [[Crouzon syndrome]]{{·}} [[Pfeiffer syndrome]]{{·}} ''intracellular signaling:'' [[Albright's hereditary osteodystrophy]]{{·}} [[Costello syndrome]]{{·}} [[Watson syndrome]]{{·}} [[Tuberous sclerosis]]{{·}} [[Marinesco–Sjögren syndrome]]{{·}} [[Cardiofaciocutaneous syndrome]]{{·}} [[Progressive osseous heteroplasia]]</div>
 
<div>TRAFFICKING: [[Arthrogryposis–renal dysfunction–cholestasis syndrome]]{{·}} [[Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome]]</div>
 
<div>CARRIER: [[BIDS syndrome]]</div>
 
<div>ENZYME: [[Neutral lipid storage disease]]{{·}} [[Noonan syndrome]]{{·}} [[Dolichol kinase deficiency]]{{·}} [[Conradi–Hünermann syndrome]]{{·}} [[CHILD syndrome]]{{·}} [[LEOPARD syndrome]]{{·}} [[X-linked recessive chondrodysplasia punctata]]{{·}} [[Schindler disease]]</div>
 
<div>CHROMOSOME: ''[[Deletion (genetics)|deletion]]'': [[18q deletion syndrome]]{{·}} [[Angelman syndrome]]/[[Prader–Willi syndrome]]</div>
 
<div>OMIM BUT NO GENE: [[Lelis syndrome]]{{·}} [[Acrogeria]]{{·}} [[Adams–Oliver syndrome]]{{·}}  [[Adducted thumbs syndrome]]{{·}} [[Atrophodermia vermiculata]]{{·}} [[Oliver–McFarlane syndrome]]{{·}} [[Rombo syndrome]]{{·}} [[Rud syndrome]]{{·}} [[Zimmermann–Laband syndrome]]{{·}} [[Incontinentia pigmenti achromians]]{{·}} [[Odonto–Tricho–Ungual–Digital–Palmar syndrome]]{{·}} [[Metageria]]{{·}} [[Westerhof syndrome]]{{·}} [[Cronkhite–Canada syndrome]]{{·}} [[Bazex–Dupré–Christol syndrome]]{{·}} [[Johnson–McMillin syndrome]]{{·}} [[Scalp–ear–nipple syndrome]]{{·}} [[Lenz–Majewski syndrome]]{{·}} [[Peeling skin syndrome]]{{·}} [[Cutis verticis gyrata]]{{·}} [[Scleroatrophic syndrome of Huriez]]{{·}} [[Hereditary sclerosing poikiloderma]]{{·}} [[Wilson–Turner syndrome]]{{·}} [[Say syndrome]]</div>
 
<div>''unsorted:''  [[Ataxia telangiectasia]]{{·}} [[Chondrodysplasia punctata]]{{·}}  [[Focal dermal hypoplasia]]{{·}} [[Klippel–Feil syndrome]]{{·}} [[Mandibuloacral dysplasia]]{{·}}  [[Multiple sulfatase deficiency]]{{·}} [[Neurofibromatosis]] ([[Neurofibromatosis type 1]], [[Neurofibromatosis type 3]], [[Neurofibromatosis type 4]], [[Segmental neurofibromatosis]]){{·}} [[Oculocerebrocutaneous syndrome]]{{·}} [[Primary hypertrophic osteoathropathy]]{{·}} [[Porokeratosis]] ([[Porokeratosis palmaris et plantaris disseminata]], [[Craniosynostosis–anal anomalies–porokeratosis syndrome]], [[Disseminated superficial actinic porokeratosis]], [[Disseminated superficial porokeratosis]], [[Linear porokeratosis]], [[Plaque-type porokeratosis]], [[Punctate porokeratosis]]){{·}} [[Progeria]]{{·}} [[Proteus syndrome]]{{·}} [[Restrictive dermopathy]]{{·}} [[Senter syndrome]]{{·}}  [[Silver–Russell syndrome]]{{·}} [[Von Hippel–Lindau syndrome]]{{·}} [[Wolf–Hirschhorn syndrome]]</div>
 
| group2 = Without OMIM
 
| list2  = [[Childhood tumor syndrome]]{{·}} [[Ectodermal dysplasia with corkscrew hairs]]{{·}} [[Fanconi syndrome]]{{·}} [[Follicular atrophoderma]]{{·}} [[Generalized trichoepithelioma]]{{·}} [[Haber syndrome]]{{·}} [[Jaffe–Campanacci syndrome]]{{·}} [[Leschke syndrome]]{{·}} [[Linear and whorled nevoid hypermelanosis]]{{·}}  [[McCusick syndrome]]{{·}} [[PIBI(D)S syndrome]]{{·}} [[Pityriasis rotunda]]{{·}} [[POEMS syndrome]]{{·}} [[Polyostotic fibrous dysplasia]]{{·}} [[Proteus-like syndrome]]{{·}} [[Relapsing linear acantholytic dermatosis]]{{·}} [[Supernumerary nipples–uropathies–Becker's nevus syndrome]]
 
}}
 
  
 
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Revision as of 00:09, 2 May 2011