Disease #03702 (PCH1B (hypoplasia, pontocerebellar, type 1b (PCH-1B)), OMIM:614678)

Official abbreviation PCH1B
Name hypoplasia, pontocerebellar, type 1b (PCH-1B)
OMIM ID 614678
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 14
Phenotype entries for this disease 14
Associated with 1 gene EXOSC3
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

14 entries on 1 page. Showing entries 1 - 14.
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00107835 - PubMed: Wan 2012 - M no - Czech 8m - - - PCH1B Pontocerebellar hypoplasia type 1 (PCH1) EXOSC3 EXOSC3 2 1 Johan den Dunnen
00107836 - PubMed: Wan 2012 - F no - Czech 8m - - - PCH1B Pontocerebellar hypoplasia type 1 (PCH1) EXOSC3 EXOSC3 2 1 Johan den Dunnen
00107837 - PubMed: Wan 2012 - M no - Czech 17m - - - PCH1B Pontocerebellar hypoplasia type 1 (PCH1) EXOSC3 EXOSC3 1 1 Johan den Dunnen
00107838 - PubMed: Wan 2012 - M no - New Caledonian >3m - - - PCH1B Pontocerebellar hypoplasia type 1 (PCH1), seen at 3m EXOSC3 EXOSC3 2 1 Johan den Dunnen
00107839 - PubMed: Wan 2012 - M no - American, European 18y - - - PCH1B floppy at birth; ocular motor apraxia; progressive muscle wasting, distal contractures; progressive microcephaly; growth retardation; global developmental delay; never reached any motor milestone or spoke; Pontocerebellar hypoplasia type 1 (PCH1) EXOSC3 EXOSC3 1 1 Johan den Dunnen
00107840 - PubMed: Wan 2012 - M no - American, European - - - - PCH1B floppy at birth; ocular motor apraxia; progressive muscle wasting, distal contractures; progressive microcephaly; growth retardation; global developmental delay; never reached any motor milestone or spoke; Pontocerebellar hypoplasia type 1 (PCH1) EXOSC3 EXOSC3 1 1 Johan den Dunnen
00107841 - PubMed: Wan 2012 - M no - American, European 16y - - - PCH1B floppy at birth; ocular motor apraxia; progressive muscle wasting, distal contractures; progressive microcephaly; growth retardation; global developmental delay; never reached any motor milestone or spoke; Pontocerebellar hypoplasia type 1 (PCH1) EXOSC3 EXOSC3 1 1 Johan den Dunnen
00107842 - PubMed: Wan 2012 - M no - American, European - - - - PCH1B floppy at birth; ocular motor apraxia; progressive muscle wasting, distal contractures; progressive microcephaly; growth retardation; global developmental delay; never reached any motor milestone or spoke; Pontocerebellar hypoplasia type 1 (PCH1) EXOSC3 EXOSC3 1 1 Johan den Dunnen
00107843 - PubMed: Wan 2012 - F no - Canadian, Cuban 3y4m - - - PCH1B Pontocerebellar hypoplasia type 1 (PCH1) EXOSC3 EXOSC3 1 1 Johan den Dunnen
00107844 - PubMed: Wan 2012 - F yes - German, Turkish - - - - PCH1B Pontocerebellar hypoplasia type 1 (PCH1) EXOSC3 EXOSC3 1 1 Johan den Dunnen
00107845 - PubMed: Wan 2012 - M yes - German, Turkish - - - - PCH1B Pontocerebellar hypoplasia type 1 (PCH1) EXOSC3 EXOSC3 1 1 Johan den Dunnen
00107846 - PubMed: Wan 2012 - F no - Australian 2y2m - - - PCH1B Pontocerebellar hypoplasia type 1 (PCH1) EXOSC3 EXOSC3 2 1 Johan den Dunnen
00107847 - PubMed: Wan 2012 - M yes - Australian, Turkish 3y - - - PCH1B Pontocerebellar hypoplasia type 1 (PCH1) EXOSC3 EXOSC3 1 1 Johan den Dunnen
00107848 - PubMed: Wan 2012 - M no - Australian 11m - - - PCH1B Pontocerebellar hypoplasia type 1 (PCH1) EXOSC3 EXOSC3 2 1 Johan den Dunnen
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