Phenotypes for disease #06174 (EDSPD2 (Ehlers-Danlos syndrome, periodontal type, 2), OMIM:617174)

12 entries on 1 page. Showing entries 1 - 12.
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Phenotype details     

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Phenotype/Onset     

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Individual ID     
0000325244 - - Premature loss of two lower incisors at four years of age, primary dentition with missing teeth 71 and 81. Gingival inflammation and probing pocket depths ≤3 mm. Furcation involvement grade III was diagnosed for deciduous molars 54, 64, 74, and 84. Lack of attached gingiva and severe gingival recession up to 6 mm was found for all primary teeth except the lower second molars. Isolated (sporadic) 05y - 04y - Nassim Louail 00435001
0000325253 - Periodontal Ehlers Danlos Syndrome - Familial, autosomal dominant - - - - Chloe Angwin 00435006
0000325257 - Periodontal Ehlers Danlos Syndrome - Familial, autosomal dominant - - - - Chloe Angwin 00435014
0000325258 - Periodontal Ehlers Danlos Syndrome - Familial, autosomal dominant - - - - Chloe Angwin 00435016
0000325261 - Periodontal Ehlers Danlos Syndrome - Familial, autosomal dominant - - - - Chloe Angwin 00435019
0000325262 - Periodontal Ehlers Danlos Syndrome - Familial, autosomal dominant - - - - Chloe Angwin 00435020
0000325264 - Periodontal Ehlers Danlos Syndrome - Familial, autosomal dominant - - - - Chloe Angwin 00435022
0000325265 - Periodontal Ehlers Danlos Syndrome - Familial, autosomal dominant - - - - Chloe Angwin 00435023
0000325266 - Periodontal Ehlers Danlos Syndrome - Familial, autosomal dominant - - - - Chloe Angwin 00435024
0000325267 - Periodontal Ehlers Danlos Syndrome - Familial, autosomal dominant - - - - Chloe Angwin 00435025
0000325277 - Periodontal Ehlers Danlos Syndrome - Familial, autosomal dominant - - - - Chloe Angwin 00435037
0000325278 - Periodontal Ehlers Danlos Syndrome - Familial, autosomal dominant - - - - Chloe Angwin 00435039
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