About: polysyndactyly

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

medical condition

Attributes	Values
rdf:type	Item
owl:sameAs	polysyndactyly
description	medical condition (en) медичний стан (uk) angeborenes orthopädisches Syndrom (de)
health specialty	wds:Q1595685-322699F9-2AA5-4BDD-A1F1-D3FB017ADD07
ICD-10	wds:Q1595685-E81EF37F-C16F-4BA3-91BE-97D6FC7F25A2
health specialty	medical genetics
ICD-10	Q70.4
rdfs:label	polysyndactyly (en) Polysyndaktylie (de) polysyndactylie (fr) پرانگشتی چسبیده (fa)
skos:prefLabel	polysyndactyly (en) Polysyndaktylie (de) polysyndactylie (fr) پرانگشتی چسبیده (fa)
name	polysyndactyly (en) Polysyndaktylie (de) polysyndactylie (fr) پرانگشتی چسبیده (fa)
instance of	wds:Q1595685-9CF56265-2548-4C5D-9B0A-4F90ED468D62
instance of	class of disease
subclass of	wds:Q1595685-0E956014-C050-4E63-8386-2185072AF1F3 wds:Q1595685-96C5BBE4-043F-418F-8F32-4F4232D6F30E
subclass of	syndactyly polydactyly
KEGG ID	wds:Q1595685-028B7476-C337-4C77-874F-E6ED9B213112
KEGG ID	http://www.kegg.jp/entry/H01226
KEGG ID	H01226
Orphanet ID	wds:Q1595685-D979BF86-05C1-4254-A884-6B8E1E2D295F
OMIM ID	wds:Q1595685-1EBBAD47-A77B-494B-BAF8-297161CAE35B
Orphanet ID	93338
OMIM ID	175690
Medical Dictionary...ory Activities ID	wds:Q1595685-A1752826-E4CA-4128-ADEA-B38DFFD5818B
Medical Dictionary...ory Activities ID	http://purl.bioontology.org/ontology/MDRFRE/10063143
Medical Dictionary...ory Activities ID	10063143
NCI Thesaurus ID	wds:Q1595685-33093724-0A57-49BF-B7AE-842609DD110F
UMLS CUI	wds:Q1595685-92EBE1B1-19C8-4AD1-87D3-82E9FB69668B
Microsoft Academic ID	wds:Q1595685-D1B9972B-2886-4D89-93E7-0AA70842FAD7
ICD-11 ID (MMS)	wds:Q1595685-3587AF1C-69BC-4EF9-89A5-22ED64C4D0F1
ICD-11 (foundation)	wds:Q1595685-A974D33C-9AE9-46A9-A312-AD734E14875E
Microsoft Academic ID	https://makg.org/entity/2779035543
NCI Thesaurus ID	C125597
UMLS CUI	C3808274
Microsoft Academic ID	2779035543
ICD-11 ID (MMS)	LB78.1
ICD-11 (foundation)	973656080
is owl:sameAs of	polysyndactyly
is about of	polysyndactyly https://de.wikipedia.org/wiki/Polysyndaktylie https://www.wikidata.org/wiki/Special:EntityData/Q1595685 Polysyndactyly https://fr.wikipedia.org/wiki/Polysyndactylie https://fa.wikipedia.org/wiki/%D9%BE%D8%B1%D8%A7%D9%86%DA%AF%D8%B4%D8%AA%DB%8C_%DA%86%D8%B3%D8%A8%DB%8C%D8%AF%D9%87
is subclass of of	crossed polysyndactyly polysyndactyly, unilateral polysyndactyly, bilateral
is subclass of of	wds:Q55781397-947d7d14-4f93-97c1-0042-f80120c51be3 wds:Q55787143-41d779df-42a9-1a50-77dc-1046e8b85111 wds:Q55787144-cf9f0a2c-4ade-01f9-9df3-c813a2841885
is main subject of	Abnormal development of the apical ectodermal ridge and polysyndactyly in Megf7-deficient mice An autosomal dominant triphalangeal thumb: polysyndactyly syndrome with variable expression in a large Indian family maps to 7q36. A complex bilateral polysyndactyly disease locus maps to chromosome 7q36 Polysyndactyly and asymptomatic hypothalamic hamartoma in mother and son: a variant of Pallister-Hall syndrome. Autosomal dominant inheritance of hypothalamic hamartoma associated with polysyndactyly: heterogeneity or variable expressivity? Regional and physical mapping studies characterizing the Greig polysyndactyly 3;7 chromosome translocation, t(3;7)(p21.1;p13). Familial polysyndactyly and craniofacial anomalies. A newborn infant with craniofacial dysmorphism and polysyndactyly (Greig's syndrome) Craniofacial abnormalities, agenesis of the corpus callosum, polysyndactyly and abnormal skin and gut development--the Curry Jones syndrome A lethal neonatal dwarfing condition with short ribs, polysyndactyly, cranial synostosis, cleft palate cardiovascular and urogenital anomalies and severe ossification defect Increasing Fgf4 expression in the mouse limb bud causes polysyndactyly and rescues the skeletal defects that result from loss of Fgf8 function Polysyndactyly and Marfan's syndrome A FAMILY WITH POLYSYNDACTYLY AND OTHER ANOMALIES A specific mutation in the distant sonic hedgehog (SHH) cis-regulator (ZRS) causes Werner mesomelic syndrome (WMS) while complete ZRS duplications underlie Haas type polysyndactyly and preaxial polydactyly (PPD) with or without triphalangeal thumb Bilateral complete polysyndactyly (type IV Haas) Heterozygous deletion at 14q22.1-q22.3 including the BMP4 gene in a patient with psychomotor retardation, congenital corneal opacity and feet polysyndactyly Polysyndactyly, short limbs, and genital malformations--a new syndrome? A male with polysyndactyly, linear skin defects and sclerocornea. Goltz syndrome versus MIDAS. Hypertelorism, proptosis, ptosis, polysyndactyly, hypospadias and normal height in 3 sibs: a new syndrome? Nevus Comedonicus Syndrome-Nevus Comedonicus Associated with Ipsilateral Polysyndactyly and Bilateral Oligodontia Compound heterozygosity for a frame shift mutation and a likely pathogenic sequence variant in the planar cell polarity—ciliogenesis gene WDPCP in a girl with polysyndactyly, coarctation of the aorta, and tongue hamartomas. Craniosynostosis. II. Coronal synostosis: its familial characteristics and associated clinical findings in 109 patients lacking bilateral polysyndactyly or syndactyly. Fibular hemimelia with polysyndactyly: a case report Micromelia, polysyndactyly, multiple malformations, and fragile bones in a stillborn child A girl with ectodermal dysplasia, choanal atresia and polysyndactyly Unilateral tibial aplasia, pre-axial polysyndactyly, vertebral anomalies and imperforate anus A new operation for syndactyly and polysyndactyly of the foot without skin grafts [Familial association of hypothalamic hamartoma and polysyndactyly] Operation for polysyndactyly of the fifth toe using Z-plasty Greig's syndrome: variable polysyndactyly associated with distinct craniofacial dymorphism Reconstruction of syndactyly and polysyndactyly of the toes with a dorsal pentagonal island flap: a technique that allows primary skin closure without the use of skin grafting. An autosomal dominant triphalangeal thumb: Polysyndactyly syndrome with variable expression in a large Indian family maps to 7q36 Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas-type polysyndactyly and Laurin-Sandrow syndrome. A syndrome of microcephaly, short stature, polysyndactyly, and dental anomalies caused by a homozygous KATNB1 mutation. Surgical Outcomes and Predictive Factors of Medial Toe Excision for Polysyndactyly of the Fifth Toe The Greig polysyndactyly craniofacial dysmorphism syndrome: Variable expression in a family Hypoplastic tibiae with postaxial polysyndactyly: a new dominant syndrome? Apert syndrome with polysyndactyly of the feet Apert syndrome with partial polysyndactyly: a proposal on the classification of acrocephalosyndactyly

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