Disease #00324 (CP (palsy, cerebral (CP)))

Official abbreviation CP
Name palsy, cerebral (CP)
OMIM ID -
Inheritance -
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene AP4M1
Associated tissues -
Disease features -
Remarks -
Date created 2014-02-15 20:10:49 +01:00 (CET)
Date last edited 2015-03-27 22:36:00 +01:00 (CET)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00011661 - PubMed: Verkerk 2009 4-generation family, 5 affecteds, unaffacted carrier parents - yes Netherlands Morrocan - - - - CP congenital spastic tetraple-gia (CST) AP4M1 AP4M1 1 5 Johan den Dunnen
00034565 - PubMed: Jameel 2014, Journal: Jameel 2014 4-generation family, 2 affected bothers, unaffected heterozygous carriers M yes Pakistan - - - - - CP see paper; erebral palsy, spastic paraplegia, intellectual disability, ... AP4M1 AP4M1 1 2 Johan den Dunnen
00034566 - PubMed: Tüysüz 2014, Journal: Tüysüz 2014 5-generation family, 2 affected sisters, unaffected heterozygous carriers F yes Turkey - - - - - CP see paper; tetraplegic cerebral palsy, intellectual disability, ... AP4M1 AP4M1 1 2 Johan den Dunnen
00034567 - PubMed: Tüysüz 2014, Journal: Tüysüz 2014 6-generation family, 2 affected sibs (F, M), unaffected heterozygous carrier parents - yes Turkey - - - - - CP see paper; tetraplegic cerebral palsy, intellectual disability, ... AP4M1 AP4M1 1 2 Johan den Dunnen
00034568 - PubMed: Tüysüz 2014, Journal: Tüysüz 2014 2-generation family, 2 affected sisters, unaffected heterozygous carrier parents F ? Turkey - - - - - CP see paper; tetraplegic cerebral palsy, intellectual disability, ... AP4B1 AP4B1 1 2 Johan den Dunnen
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