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Phenotypes for disease #02795 (LGMDR10;LGMD2J (dystrophy, muscular, limb-girdle, autosomal recessive, type 10 (LGMD2J)), OMIM:608807)
Legend
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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all entries matching the year 2020
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Date
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Date
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Date
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Date
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Date
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Date
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all entries on or after June 15th, 2020
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Date
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all entries in 2019 or 2020, and before March, 2020
Numeric
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all entries exactly matching 23
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Numeric
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all entries exactly matching 23 or 24
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Numeric
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all entries not exactly matching 23
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Numeric
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all entries lower than 23
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Numeric
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all entries lower than, or equal to, 23
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Numeric
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Numeric
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all entries higher than, or equal to, 23
combination
Numeric
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all entries with values from 20 to 29, but not equal to 23
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all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
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all entries containing 'Asian' but not containing 'Caucasian'
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all entries containing 'Asian' or 'African', but not containing 'Caucasian'
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all entries containing 'South Asian', but not containing 'South East Asian'
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31 entries on 1 page. Showing entries 1 - 31.
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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
0000044580
severe TMD; IHC no M8/M9-TTN epitopes but A169/A170 normal, CAPN3 severly reduced
-
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00057949
0000044981
-
-
-
-
-
-
-
-
-
Johan den Dunnen
00058350
0000044982
-
-
-
-
-
-
-
-
-
Johan den Dunnen
00058351
0000044983
-
-
-
-
-
-
-
-
-
Johan den Dunnen
00058352
0000044984
-
-
-
-
-
-
-
-
-
Johan den Dunnen
00058353
0000066700
Distal muscle weakness
-
-
Familial, autosomal recessive
-
-
-
-
-
Ana Topf
00087088
0000066765
-
-
-
Familial, autosomal recessive
49y
-
44y
-
-
Ana Topf
00087240
0000066766
-
-
-
Familial, autosomal recessive
30y
-
25y
-
-
Ana Topf
00087241
0000066767
-
-
-
Familial, autosomal recessive
48y
-
?
-
-
Ana Topf
00087243
0000066768
-
-
-
Familial, autosomal recessive
47y
-
25y
-
-
Ana Topf
00087245
0000066769
-
-
-
Familial, autosomal recessive
44y
-
39y
-
-
Ana Topf
00087247
0000066770
-
-
-
Familial, autosomal recessive
25y
-
22y
-
-
Ana Topf
00087248
0000066772
-
-
-
Familial, autosomal recessive
32y
-
28y
-
-
Ana Topf
00087250
0000066773
-
-
-
Familial, autosomal recessive
27y
-
19y
-
-
Ana Topf
00087251
0000066774
-
-
-
Familial, autosomal recessive
29y
-
25y
-
-
Ana Topf
00087252
0000066775
-
-
-
Familial, autosomal recessive
53y
-
40y
-
-
Ana Topf
00087253
0000066776
-
-
-
Familial, autosomal recessive
15y
-
14y
-
-
Ana Topf
00087254
0000066777
-
-
-
Familial, autosomal recessive
44y
-
40y
-
-
Ana Topf
00087244
0000066778
-
-
-
Familial, autosomal recessive
43y
-
28y
-
-
Ana Topf
00087255
0000226943
-
-
-
Isolated (sporadic)
-
-
03y
Delayed early motor development
-
Marco Savarese
00299633
0000226944
Childhood/early-adult onset distal myopathy
-
-
Familial, autosomal recessive
-
-
08y?
Myalgia
-
Marco Savarese
00299634
0000226945
Childhood/early-adult onset distal myopathy
-
-
Isolated (sporadic)
-
-
18y?
Reduced ankle DF
-
Marco Savarese
00299635
0000226946
Childhood/early-adult onset distal myopathy
-
-
Familial, autosomal recessive
-
-
01y?
-
-
Marco Savarese
00299636
0000226947
Childhood/early-adult onset distal myopathy
-
-
Isolated (sporadic)
-
-
-
-
-
Marco Savarese
00299637
0000227499
Childhood/early-adult onset distal myopathy
-
-
Isolated (sporadic)
-
-
30y?
Weakness, muscle pain
-
Marco Savarese
00300173
0000227501
Childhood/early-adult onset distal myopathy
-
-
Isolated (sporadic)
-
-
16y?
Asymmetrical bilateral foot drop
-
Marco Savarese
00300174
0000227502
Childhood/early-adult onset distal myopathy
-
-
Isolated (sporadic)
-
-
20y?
Distal lower limb weakness and myoglobinuria
-
Marco Savarese
00300175
0000227503
Childhood/early-adult onset distal myopathy
-
-
Isolated (sporadic)
-
-
>30y
Difficulty in walking
-
Marco Savarese
00300176
0000227505
hyperCKemia
-
-
Familial, autosomal recessive
-
-
-
hyperCKemia
-
Marco Savarese
00300177
0000250503
Limb-girdle muscular dystrophy HP:0006785
-
-
Isolated (sporadic)
-
-
-
-
-
Svetlana Gorokhova
00332316
0000274648
delayed motor development; muscular hypotonia; lactic acidosis (Neurological)
-
LGMD type 2J
Familial
-
-
-
-
-
LOVD
00380795
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