Disease #07011 (EDSPD1 (Ehlers-Danlos syndrome, periodontal type, 1), OMIM:130080)

Official abbreviation EDSPD1
Name Ehlers-Danlos syndrome, periodontal type, 1
OMIM ID 130080
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene C1R
Associated tissues -
Disease features -
Remarks -
Date created 2023-05-01 17:52:31 +02:00 (CEST)
Date last edited N/A


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00435230 - PubMed: Kapferer-Seebacher et al., 2016Journal: Kapferer-Seebacher 2016 - F no (Austria) - - - - - EDSPD1 The cardinal clinical feature is severe early-onset periodontitis with marked gingival recessions that in some individuals affects primary teeth C1S C1S 1 5 Christian Drouet
00435231 - Journal: Kapferer-Seebacher 2016 - M - (Austria) - - - - - EDSPD1 Proband presenting with extensive gingival inflammation in response to mild dental plaque accumulation and early-onset periodontitis characterized by a rapid destruction of the periodontal attachment apparatus in the teens. C1S C1S 1 4 Christian Drouet
00435331 1 PubMed: Grobner et al., 2019 - ? no Australia - - - - - EDSPD1 early severe and rapidly progressing periodontal destruction and variable connective tissue abnormalities C1R C1R 1 1 Nassim Louail
00435332 Fam2 PubMed: Kapferer-Seebacher 2016, Journal: Kapferer-Seebacher 2016 - F no - - - - - - EDSPD1 early severe and rapidly progressing periodontal destruction and variable connective tissue abnormalities C1R C1R 1 1 Nassim Louail
00435333 Fam3 PubMed: Kapferer-Seebacher 2016, Journal: Kapferer-Seebacher 2016 - F no - - - - - - EDSPD1 early severe and rapidly progressing periodontal destruction and variable connective tissue abnormalities C1R C1R 1 1 Nassim Louail
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