Aarskog–Scott syndrome
Aarskog–Scott syndrome is a rare disease inherited as X-linked and characterized by short stature, facial abnormalities, skeletal and genital anomalies. This condition mainly affects males, although females may have mild features of the syndrome.
known for
AarskogAarskog-Scott syndromeAarskog Scott SyndromeAarskog syndromeAndrogen insensitivity syndromeBrachymetatarsiaClinodactylyDagfinn AarskogFGD1FYVE, RhoGEF and PH domain containingFacial-digital-genital syndromeFaciodigitogenital syndromeFaciogenital dysplasiaFetal alcohol spectrum disorderGlossary of medicineInterdigital webbingList of OMIM disorder codesList of abbreviations for diseases and disordersList of diseases (A)List of eponymous diseasesList of genetic disordersList of geneticistsList of syndromesLujan–Fryns syndromeSex linkageShawl scrotumShawl scrotum syndromeSingle transverse palmar creaseWebbed toesWidow's peak
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known for
primaryTopic
Aarskog–Scott syndrome
Aarskog–Scott syndrome is a rare disease inherited as X-linked and characterized by short stature, facial abnormalities, skeletal and genital anomalies. This condition mainly affects males, although females may have mild features of the syndrome.
has abstract
A síndrome de Aarskog, também ...... de forma independente em 1971.
@pt
Aarskogs syndrom, även kallat ...... gare hos pojkar med syndromet.
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Aarskogův-Scottův syndrom je v ...... agnózy je genetické vyšetření.
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Aarskog–Scott syndrome is a ra ...... mild features of the syndrome.
@en
Das Aarskog-Syndrom ist auch u ...... Pädiater Charles I. Jr. Scott.
@de
El síndrome Aarskog o síndrome ...... sde su descubrimiento en 1970.
@es
La sindrome di Aarskog è una m ...... tarietà eterosomica dominante.
@it
Le syndrome d'Aarskog ou syndr ...... est situé sur le chromosome X.
@fr
Sindrom Aarskog-Scott atau dis ...... lain menjabarkan sindrom ini.
@in
Zespół Aarskoga (dysplazja twa ...... y kośćca i narządów płciowych.
@pl
DiseasesDB
ICD10
ICD9
medical cause
MedlinePlus
MeSH ID
OMIM id
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page length (characters) of wiki page
Wikipage revision ID
999.157.704
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causes
Genetic
@en
deaths
2.0828016E9
DiseasesDB
ICD
MedlinePlus
MeshID
name
Aarskog–Scott syndrome / Aarskog Syndrome
@en
OMIM
Orphanet
symptoms
Broad hands and feet, wide set eyes, low set ears, drooping lower lip
@en
synonyms
Faciodigitogenital syndrome , ...... isease, Scott Aarskog syndrome
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A síndrome de Aarskog, também ...... ar traços brandos da síndrome.
@pt
Aarskogs syndrom, även kallat ...... gare hos pojkar med syndromet.
@sv
Aarskogův-Scottův syndrom je v ...... agnózy je genetické vyšetření.
@cs
Aarskog–Scott syndrome is a ra ...... mild features of the syndrome.
@en
Das Aarskog-Syndrom ist auch u ...... Pädiater Charles I. Jr. Scott.
@de
El síndrome Aarskog o síndrome ...... sde su descubrimiento en 1970.
@es
La sindrome di Aarskog è una m ...... tarietà eterosomica dominante.
@it
Le syndrome d'Aarskog ou syndr ...... est situé sur le chromosome X.
@fr
Sindrom Aarskog-Scott atau dis ...... lain menjabarkan sindrom ini.
@in
Zespół Aarskoga (dysplazja twa ...... y kośćca i narządów płciowych.
@pl
label
Aarskog-Syndrom
@de
Aarskogs syndrom
@sv
Aarskogův–Scottův syndrom
@cs
Aarskog–Scott syndrome
@en
Sindrom Aarskog-Scott
@in
Sindrome di Aarskog
@it
Syndrome d'Aarskog
@fr
Síndrome de Aarskog
@pt
Síndrome de Aarskog-Scott
@es
Zespół Aarskoga
@pl
sameAs
wasDerivedFrom
isPrimaryTopicOf
name
Aarskog–Scott syndrome / Aarskog Syndrome
@en