Disease #02985 (HPE7 (holoprosencephaly, type 7 (HPE-7)), OMIM:610828)

Official abbreviation HPE7
Name holoprosencephaly, type 7 (HPE-7)
OMIM ID 610828
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 7
Phenotype entries for this disease 7
Associated with 1 gene PTCH1
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

7 entries on 1 page. Showing entries 1 - 7.
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00063332 - PubMed: Ming 2002 - - - - - - - - - HPE7 - PTCH1 PTCH1 1 1 Michel van Geel
00063338 - PubMed: Ribeiro 2006 - - - - - - - - - HPE7 - PTCH1 PTCH1 1 1 Michel van Geel
00063363 - PubMed: Ming 2002 - - - - - - - - - HPE7 - PTCH1 PTCH1 1 1 Michel van Geel
00063365 - PubMed: Ribeiro 2006 - - - - - - - - - HPE7 - PTCH1 PTCH1 1 1 Michel van Geel
00063372 - PubMed: Ming 2002 - - - - - - - - - HPE7 - PTCH1 PTCH1 1 1 Michel van Geel
00063375 - PubMed: Ribeiro 2006 - - - - - - - - - HPE7 - PTCH1 PTCH1 1 1 Michel van Geel
00063388 - PubMed: Ming 2002 - - - - - - - - - HPE7 - PTCH1 PTCH1 1 1 Michel van Geel
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