Global Variome shared LOVD
TLR7 (toll-like receptor 7)
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Phenotypes for disease #02492 (LGMDR4;LGMD2E (dystrophy, muscular, limb-girdle, autosomal recessive, type 4 (LGMD2E)), OMIM:604286)
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Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
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
Protein
: result from protein staining
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Date
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Date
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19 entries on 1 page. Showing entries 1 - 19.
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How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000051876
mild limb-girdle muscular dystrophy (HP:0006785), cardiomyopathy (HP:0001638), proximal muscle weakness (HP:0003701)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00072171
0000051877
mild limb-girdle muscular dystrophy (HP:0006785), cardiomyopathy (HP:0001638), proximal muscle weakness (HP:0003701)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00072173
0000051878
mild limb-girdle muscular dystrophy (HP:0006785), cardiomyopathy (HP:0001638), proximal muscle weakness (HP:0003701)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00072174
0000051879
cardiomyopathy (HP:0001638), proximal muscle weakness (HP:0003701)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00072175
0000051880
proximal muscle weakness (HP:0003701)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00072176
0000051882
mild limb-girdle muscular dystrophy (HP:0006785), proximal muscle weakness (HP:0003701)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00072177
0000051883
severe limb-girdle muscular dystrophy (HP:0006785), cardiomyopathy (HP:0001638), proximal muscle weakness (HP:0003701), distal muscle weakness (HP:0002460)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00072179
0000051884
severe limb-girdle muscular dystrophy (HP:0006785), cardiomyopathy (HP:0001638), proximal muscle weakness (HP:0003701), distal muscle weakness (HP:0002460)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00072180
0000051886
severe limb-girdle muscular dystrophy (HP:0006785), cardiomyopathy (HP:0001638), proximal muscle weakness (HP:0003701), distal muscle weakness (HP:0002460)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00072181
0000051887
mild limb-girdle muscular dystrophy (HP:0006785), proximal muscle weakness (HP:0003701), distal muscle weakness (HP:0002460)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00072182
0000051888
mild limb-girdle muscular dystrophy (HP:0006785), cardiomyopathy (HP:0001638), proximal muscle weakness (HP:0003701), distal muscle weakness (HP:0002460)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00072184
0000051889
mild limb-girdle muscular dystrophy (HP:0006785), no cardiomyopathy (-HP:0001638), proximal muscle weakness (HP:0003701), distal muscle weakness (HP:0002460)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00072185
0000051894
severe limb-girdle muscular dystrophy (HP:0006785), proximal muscle weakness (HP:0003701), distal muscle weakness (HP:0002460)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00072190
0000051896
proximal muscle weakness (HP:0003701)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00072191
0000051899
severe or mild limb-girdle muscular dystrophy (HP:0006785), cardiomyopathy (HP:0001638), proximal muscle weakness (HP:0003701), distal muscle weakness (HP:0002460)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00072194
0000051901
severe limb-girdle muscular dystrophy (HP:0006785), cardiomyopathy (HP:0001638), proximal muscle weakness (HP:0003701), distal muscle weakness (HP:0002460)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00072196
0000051902
severe limb-girdle muscular dystrophy (HP:0006785), cardiomyopathy (HP:0001638), proximal muscle weakness (HP:0003701), distal muscle weakness (HP:0002460)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00072197
0000051905
proximal muscle weakness (HP:0003701)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00072200
0000281597
HP:0003701 (proximal muscle weakness), HP:0030234 (highly elevated creatine kinase, 7646 U/L); difficulty getting up from ground and climbing stairs, calf hypertrophy; most-affected muscles hip and knee extensors, ankle dorsiflexors; no cardiac involvement; 12y-ambulant
limb-girdle muscular dystrophy
LGMD2E
Familial, autosomal recessive
12y
-
11y
-
IHC no SGCB
Micaela Carcione
00388003
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