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Clements SE, Techanukul T, Holden ST, et al. (September 2010). "Rapp–Hodgkin and Hay–Wells ectodermal dysplasia syndromes represent a variable spectrum of the same genetic disorder".
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GeneReviews/NCBI/NIH/UW entry on
Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate Syndrome or AEC Syndrome, Hay–Wells Syndrome. Includes: Rapp–Hodgkin Syndrome
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158:"Anhidrotic ectodermal dysplasia: autosomal dominant inheritance with palate and lip anomalies"
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disorder due to a P63 gene mutation. However, it was recently shown to the same disease as
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This condition is inherited in an autosomal dominant manner.
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1231:Ectrodactyly–ectodermal dysplasia–cleft syndrome 3
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1123:Yemenite deaf-blind hypopigmentation syndrome
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18:Rapp–Hodgkin ectodermal dysplasia syndrome
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727:Posterior polymorphous corneal dystrophy
557:Autoimmune polyendocrine syndrome type 1
918:Anterior segment mesenchymal dysgenesis
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450:X-linked adrenal hypoplasia congenita
156:Rapp RS, Hodgkin WE (December 1968).
7:
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502:Greig cephalopolysyndactyly syndrome
79:It was first characterized in 1968.
68:was formerly thought to be a unique
876:Iridogoniodysgenesis, dominant type
1329:. You can help Knowledge (XXG) by
25:
890:Lymphedema–distichiasis syndrome
486:Tricho–rhino–phalangeal syndrome
460:Familial partial lipodystrophy 3
127:10.1111/j.1365-2133.2010.09859.x
1154:(0) Other transcription factors
445:Estrogen insensitivity syndrome
413:Androgen insensitivity syndrome
1035:Hyperimmunoglobulin E syndrome
440:PHA1AD pseudohypoaldosteronism
1:
1297:Atrichia with papular lesions
1004:Popliteal pterygium syndrome
946:Enlarged vestibular aqueduct
785:Waardenburg syndrome 1&3
570:(3) Helix-turn-helix domains
329:relating to deficiencies of
94:List of cutaneous conditions
1104:Premature ovarian failure 7
960:Premature ovarian failure 3
832:Congenital hypothyroidism 2
1402:
1315:
1251:Transcription coregulators
1021:with minor groove contacts
408:Thyroid hormone resistance
1273:Rubinstein–Taybi syndrome
1099:SRY XY gonadal dysgenesis
904:Bamforth–Lazarus syndrome
516:Duane-radial ray syndrome
465:SF1 XY gonadal dysgenesis
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37:
1141:Cleidocranial dysostosis
358:Saethre–Chotzen syndrome
1118:Waardenburg syndrome 4c
818:Coloboma of optic nerve
666:Tooth and nail syndrome
506:Pallister–Hall syndrome
1061:Ulnar–mammary syndrome
1019:(4) β-Scaffold factors
999:Van der Woude syndrome
531:Townes–Brocks syndrome
404:Intracellular receptor
89:Punctate porokeratosis
1235:Limb–mammary syndrome
1223:Rapp–Hodgkin syndrome
1195:Pitt–Hopkins syndrome
771:Papillorenal syndrome
746:Mowat–Wilson syndrome
652:Nail–patella syndrome
536:Acrocallosal syndrome
66:Rapp–Hodgkin syndrome
33:Rapp–Hodgkin syndrome
1386:Genodermatoses stubs
1077:Campomelic dysplasia
1056:Li–Fraumeni syndrome
541:Myotonic dystrophy 2
511:Denys–Drash syndrome
331:transcription factor
871:Axenfeld syndrome 3
685:Axenfeld syndrome 1
624:SPD1 synpolydactyly
389:DNA-binding domains
291:OMIM entries on AEC
174:10.1136/jmg.5.4.269
1227:Hay–Wells syndrome
1051:Holt–Oram syndrome
813:Gillespie syndrome
732:Fuchs' dystrophy 3
610:Currarino syndrome
263:External resources
74:Hay–Wells syndrome
70:autosomal dominant
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435:Kennedy's disease
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353:Feingold syndrome
339:(1) Basic domains
327:Genetic disorders
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27:Medical condition
16:(Redirected from
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387:(2) Zinc finger
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333:or coregulators
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203:Further reading
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1331:expanding it
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1259:Coactivator:
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121:(3): 624–9.
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1370:Categories
100:References
1181:Ungrouped
53:Specialty
272:Orphanet
143:44866051
135:20491771
83:See also
932:ACD/MPV
253:C535289
192:5713637
183:1468665
1267:CREBBP
1087:MODY 5
1082:MODY 3
846:STHAG3
799:MODY 9
707:POU3F4
699:DFNA15
693:POU4F3
638:MODY 4
618:HOXD13
526:MRX 89
521:MODY 7
455:MODY 1
242:129400
190:
180:
141:
133:
1321:This
1209:TNDM1
1203:ZFP57
1112:SOX10
968:FOXP3
954:FOXL2
940:FOXI1
926:FOXF1
912:FOXE3
898:FOXE1
884:FOXC2
865:FOXC1
713:DFNX2
679:PITX2
646:LMX1B
139:S2CID
1327:stub
1239:OFC8
1217:TP63
1189:TCF4
1134:4.11
993:IRF6
974:IPEX
840:PAX9
826:PAX8
807:PAX6
793:PAX4
779:PAX3
765:PAX2
740:ZEB2
721:ZEB1
671:OFC5
660:MSX1
632:PDX1
604:MNX1
428:CAIS
423:MAIS
418:PAIS
277:3022
248:MeSH
237:OMIM
188:PMID
131:PMID
1161:0.6
1093:SF1
1070:4.7
1044:4.3
1028:4.2
985:3.5
857:3.3
757:3.2
585:ARX
577:3.1
550:2.5
495:2.3
474:2.2
406:):
396:2.1
367:1.3
346:1.2
178:PMC
170:doi
123:doi
119:163
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