Disease #00453 (Perry (Perry syndrome), OMIM:168605)

Official abbreviation Perry
Name Perry syndrome
OMIM ID 168605
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 8
Phenotype entries for this disease 8
Associated with 1 gene DCTN1
Associated tissues -
Disease features -
Remarks -


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00017879 - PubMed: Farrer 2009 3-generation family, 3 affecteds (2F, M) - ? Turkey - - 0 - - Perry see paper DCTN1 DCTN1 1 3 Johan den Dunnen
00017880 - PubMed: Farrer 2009 5-generation family, 11 affecteds (2F, 9M) - ? Canada - - 0 - - Perry see paper DCTN1 DCTN1 1 11 Johan den Dunnen
00017881 - PubMed: Farrer 2009 3-generation family, 7 affecteds (5F, 2M) - ? France - - 0 - - Perry see paper DCTN1 DCTN1 1 7 Johan den Dunnen
00017882 - PubMed: Farrer 2009 3-generation family, 3 affecteds (2F, M) - ? United States Hawaii - 0 - - Perry see paper DCTN1 DCTN1 1 3 Johan den Dunnen
00017883 - PubMed: Farrer 2009 3-generation family, 6 affecteds (3F, 3M) - ? United Kingdom (Great Britain) - - 0 - - Perry see paper DCTN1 DCTN1 1 6 Johan den Dunnen
00017884 - PubMed: Farrer 2009 3-generation family, 8 affecteds (F, 7M) - ? Japan - - 0 - - Perry see paper DCTN1 DCTN1 1 8 Johan den Dunnen
00017885 - PubMed: Farrer 2009 4-generation family, 5 affecteds (2F, 3M) - ? United States - - 0 - - Perry see paper DCTN1 DCTN1 2 5 Johan den Dunnen
00017886 - PubMed: Farrer 2009 3-generation family, 4 affecteds (3F, M) - ? Japan - - 0 - - Perry see paper DCTN1 DCTN1 2 4 Johan den Dunnen
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