Disease #00741 (SGS (Schinzel-Giedion midface retraction syndrome (SGS)), OMIM:269150)

Official abbreviation SGS
Name Schinzel-Giedion midface retraction syndrome (SGS)
OMIM ID 269150
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 17
Phenotype entries for this disease 3
Associated with 1 gene SETBP1
Associated tissues -
Disease features autosomal dominant
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

17 entries on 1 page. Showing entries 1 - 17.
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00081091 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - SGS Schinzel-Giedion midface retraction syndrome (OMIM:269150) SETBP1 SETBP1 1 1 Daniel Trujillano
00207319 - - - M - - European - - - - SGS - SETBP1 SETBP1 1 1 LOVD
00207320 - - - F - - European - - - - SGS - SETBP1 SETBP1 1 1 LOVD
00207321 - - - M - - European - - - - SGS - SETBP1 SETBP1 1 1 LOVD
00207322 - - - F - - European - - - - SGS - SETBP1 SETBP1 1 1 LOVD
00207323 - - - F - - European - - - - SGS - SETBP1 SETBP1 1 1 LOVD
00207324 - - - F - - European - - - - SGS - SETBP1 SETBP1 1 1 LOVD
00207325 - - - M - - European - - - - SGS - SETBP1 SETBP1 1 1 LOVD
00207326 - - - F - - European - - - - SGS - SETBP1 SETBP1 1 1 LOVD
00207327 - - - M - - European - - - - SGS - SETBP1 SETBP1 1 1 LOVD
00207328 - - - F - - European - - - - SGS - SETBP1 SETBP1 1 1 LOVD
00207329 - - - M - - European - - - - SGS - SETBP1 SETBP1 1 1 LOVD
00207330 - - - M - - European - - - - SGS - SETBP1 SETBP1 1 1 LOVD
00289344 1123 - - M no Italy - 01y - - - SGS - SETBP1 SETBP1 1 1 Pietro Palumbo
00315902 MR466_01 - - F no Italy - - - - - SGS High forehead, Prominent forehead, Intellectual Disability, severe, Absent speech, seizures - SETBP1 1 1 Emanuela Leonardi
00391858 241P - - F no Spain - - - - - ID, MRD29, SGS - - SETBP1 1 1 Alejandro Brea-Fernández
00401306 083P - - M no Spain - - - - - ID, MRD29, SGS - - SETBP1 1 1 Alejandro Brea-Fernández
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