Disease #05108 (ECTDO (dysplasia, ectodermal, with oligodontia (ECTDO)))

Official abbreviation ECTDO
Name dysplasia, ectodermal, with oligodontia (ECTDO)
OMIM ID -
Inheritance -
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene KREMEN1
Associated tissues -
Disease features -
Remarks -
Date created 2015-12-30 01:21:12 +01:00 (CET)
Date last edited N/A


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00056411 - Issa EJHG2016 proband family SO1 M yes Palestine Palestinian - - please see Issa et al EJHG2016 - ECTDO ectodermal dysplasia (HP:0000968), oligodontia (HP:0000677) KREMEN1 KREMEN1 1 1 Mary-Claire King
00056428 - Issa EJHG2016 - - yes Palestine Palestinian - - please see Issa et al EJHG2016 - ECTDO ectodermal dysplasia (HP:0000968), oligodontia (HP:0000677) KREMEN1 KREMEN1 1 1 Mary-Claire King
00056429 - Issa EJHG2016 - - yes Palestine Palestinian - - please see Issa et al EJHG2016 - ECTDO ectodermal dysplasia (HP:0000968), oligodontia (HP:0000677) KREMEN1 KREMEN1 1 1 Mary-Claire King
00056430 - Issa EJHG2016 - - yes Palestine Palestinian - - please see Issa et al EJHG2016 - ECTDO ectodermal dysplasia (HP:0000968), oligodontia (HP:0000677) KREMEN1 KREMEN1 1 1 Mary-Claire King
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