Disease #03554 (OCCM (cortical malformations, occipital), OMIM:614115)

Official abbreviation OCCM
Name cortical malformations, occipital
OMIM ID 614115
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene LAMC3
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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00107881 - PubMed: Barak 2011 parents first-cousin F yes Turkey - - - - - OCCM Cortical malformation; occipital pachygyria LAMC3 LAMC3 1 1 Johan den Dunnen
00107882 - PubMed: Barak 2011 - F yes Turkey - - - - - OCCM Cortical malformation; occipital pachygyria LAMC3 LAMC3 1 1 Johan den Dunnen
00107883 - PubMed: Barak 2011 - F yes Turkey - - - - - OCCM Cortical malformation; occipital pachygyria LAMC3 LAMC3 2 1 Johan den Dunnen
00373741 iw001 - - F no China Chinese - - - - OCCM HP:0001263; HP:0001999; HP:0001249; HP:0002098; HP:0001252; HP:0000954; HP:0001655; HP:0008081; HP:0000316 LAMC3 LAMC3 1 1 Wenjuan Qiu
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