Global Variome shared LOVD
LTB4R2 (leukotriene B4 receptor 2)
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Phenotypes for disease #06174 (EDSPD2 (Ehlers-Danlos syndrome, periodontal type, 2), OMIM:617174)
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Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
Inheritance
: Indicates the inheritance of the phenotype in the family; unknown, familial (autosomal/X-linked, dominant/ recessive), paternal (Y-linked), maternal (mitochondrial), isolated (sporadic) or complex
All options:
Unknown
Familial
Familial, autosomal dominant
Familial, autosomal recessive
Familial, X-linked
Familial, X-linked dominant
Familial, X-linked dominant, male sparing
Familial, X-linked recessive
Paternal, Y-linked
Maternal, mitochondrial
Isolated (sporadic)
Di-genic
Complex
- = Not applicable
Age/Examination
: age at which the individual was examined.
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Diagnosis
: age diagnosis was confirmed
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Onset
: Age first symptoms disease appeared in individual:
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Phenotype/Onset
: individual's phenotype at Age/Onset described using HPO
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12 entries on 1 page. Showing entries 1 - 12.
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How to query
Phenotype ID
Diagnosis/Initial
Diagnosis/Definite
Phenotype details
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Owner
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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