Disease #00869 (3MC2 (3MC syndrome, type 2 (3MC2)), OMIM:265050)

Official abbreviation 3MC2
Name 3MC syndrome, type 2 (3MC2)
OMIM ID 265050
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 8
Phenotype entries for this disease 7
Associated with 1 gene COLEC11
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

8 entries on 1 page. Showing entries 1 - 8.
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00079986 - PubMed: Olson 2015 - F no Afghanistan - - - - - 3MC2, AAT4, AAT8 - GLDC GLDC 1 1 Johan den Dunnen
00106633 - PubMed: Rooryck 2011 Family MC11 - - Italy - - - - - 3MC2 Carnevale COLEC11 COLEC11 1 1 Johan den Dunnen
00106634 - PubMed: Rooryck 2011 Family MC4 - - Afghanistan - - - - - 3MC2 Malpuech or Michels COLEC11 COLEC11 1 1 Johan den Dunnen
00106635 - PubMed: Rooryck 2011 Family MC4 - - Afghanistan - - - - - 3MC2 Malpuech or Michels COLEC11 COLEC11 1 1 Johan den Dunnen
00106636 - PubMed: Rooryck 2011 Family MC9 - - Pakistan - - - - - 3MC2 Malpuech COLEC11 COLEC11 1 1 Johan den Dunnen
00106637 - PubMed: Rooryck 2011 Family MC8 - - Saudi Arabia - - - - - 3MC2 Carnevale COLEC11 COLEC11 1 1 Johan den Dunnen
00106638 - PubMed: Rooryck 2011 Family MC2 - - Bangladesh - - - - - 3MC2 Malpuech COLEC11 COLEC11 1 1 Johan den Dunnen
00106639 - PubMed: Rooryck 2011 Family MC2 - - Bangladesh - - - - - 3MC2 Malpuech COLEC11 COLEC11 1 1 Johan den Dunnen
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