Disease #02328 (EDM3 (dysplasia, epiphyseal, multiple, type 3 (EDM-3)), OMIM:600969)

Official abbreviation EDM3
Name dysplasia, epiphyseal, multiple, type 3 (EDM-3)
OMIM ID 600969
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 1
Associated with 1 gene COL9A3
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

4 entries on 1 page. Showing entries 1 - 4.
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00248490 - - 4-generation family, 7 affecteds - - - - - - - - EDM3 - COL9A3 COL9A3 1 7 LOVD
00248492 - - 3-generation family, 3 affecteds - - - - - - - - EDM3 - COL9A3 COL9A3 1 3 LOVD
00248493 - - 4-generation family, 11 affecteds - - - - - - - - EDM3 - COL9A3 COL9A3 1 11 LOVD
00248494 - - 3-generation family, 5 affecteds - - Japan - - - - - EDM3 - COL9A3 COL9A3 1 5 LOVD
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