Disease #01810 (GPHYSD1 (Geleophysic dysplasia), OMIM:231050)

Official abbreviation GPHYSD1
Name Geleophysic dysplasia
OMIM ID 231050
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 14
Phenotype entries for this disease -
Associated with 1 gene ADAMTSL2
Associated tissues -
Disease features -
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

14 entries on 1 page. Showing entries 1 - 14.
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00250198 - PubMed: Allali et al 2011 - - - France - - - - - GPHYSD1 - ADAMTSL2 ADAMTSL2 2 1 LOVD
00250199 - PubMed: Allali et al 2011 - - - France - - - - - GPHYSD1 - ADAMTSL2 ADAMTSL2 1 1 LOVD
00250200 - PubMed: Allali et al 2011 - - - France - - - - - GPHYSD1 - ADAMTSL2 ADAMTSL2 1 1 LOVD
00250201 - PubMed: Allali et al 2011 - - - Japan - - - - - GPHYSD1 - ADAMTSL2 ADAMTSL2 1 1 LOVD
00250202 - PubMed: Allali et al 2011 - - yes Italy - - - - - GPHYSD1 - ADAMTSL2 ADAMTSL2 1 1 LOVD
00250203 - PubMed: Allali et al 2011 - - - France - - - - - GPHYSD1 - ADAMTSL2 ADAMTSL2 2 1 LOVD
00250204 - PubMed: Allali et al 2011 sib of patient #33 - - England - - - - - GPHYSD1 - ADAMTSL2 ADAMTSL2 2 1 LOVD
00250205 - PubMed: Allali et al 2011 sib of patient #32 - - England - - - - - GPHYSD1 - ADAMTSL2 ADAMTSL2 2 1 LOVD
00250206 - PubMed: Allali et al 2011 - - - England - - - - - GPHYSD1 - ADAMTSL2 ADAMTSL2 2 1 LOVD
00250207 - PubMed: Allali et al 2011 - - - France - - - - - GPHYSD1 - ADAMTSL2 ADAMTSL2 2 1 LOVD
00250208 - PubMed: Allali et al 2011 - - yes Turkey - - - - - GPHYSD1 - ADAMTSL2 ADAMTSL2 2 1 LOVD
00250209 - PubMed: Allali et al 2011 cousin of patients #21 and #24 - yes Pakistan - - - - - GPHYSD1 - ADAMTSL2 ADAMTSL2 2 1 LOVD
00250210 - PubMed: Allali et al 2011 cousin of patients #17 and #24 - yes Pakistan - - - - - GPHYSD1 - ADAMTSL2 ADAMTSL2 2 1 LOVD
00250211 - PubMed: Allali et al 2011 cousin of patients #17 and #21 - yes Pakistan - - - - - GPHYSD1 - ADAMTSL2 ADAMTSL2 2 1 LOVD
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