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Phenotypes for disease #03021 (LGMDR12;LGMD2L (dystrophy, muscular, limb-girdle, autosomal recessive, type 12 (LGMD2L)), OMIM:611307)
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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
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' 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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38 entries on 1 page. Showing entries 1 - 38.
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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
0000058492
iliopsoas MRC 4, quadriceps atrophy, quadriceps MRC 5, calf muscles no weakness, no distal weakness ; raised CPK (HP:0003236) 1649; >68y walking (-HP:0006957)
-
-
Isolated (sporadic)
68y
-
0y
-
-
Johan den Dunnen
00078733
0000058493
iliopsoas MRC 4, quadriceps atrophy, quadriceps MRC 4.5, calf muscles mild atrophy, no distal weakness ; raised CPK (HP:0003236) 1032; >67y walking (-HP:0006957)
-
-
Isolated (sporadic)
67y
-
40y
-
-
Johan den Dunnen
00078734
0000058494
iliopsoas MRC 4, quadriceps atrophy, quadriceps MRC 4, calf muscles mild atrophy, no distal weakness ; raised CPK (HP:0003236) 1156; >65y walking (-HP:0006957)
-
-
Isolated (sporadic)
65y
-
37y
-
-
Johan den Dunnen
00078735
0000058495
iliopsoas MRC 4, quadriceps atrophy, quadriceps MRC 5, calf muscles mild atrophy, no distal weakness ; raised CPK (HP:0003236) 6000; >47y walking (-HP:0006957)
-
-
Isolated (sporadic)
47y
-
20y
-
-
Johan den Dunnen
00078736
0000058496
deceased
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00078737
0000058497
iliopsoas MRC 4, quadriceps atrophy, quadriceps MRC 5, calf muscles atrophy, distal weakness calf muscles 4/5; raised CPK (HP:0003236) 8081; >43y walking (-HP:0006957)
-
-
Familial, autosomal recessive
43y
-
20y
-
-
Johan den Dunnen
00078738
0000058498
iliopsoas MRC 4.5, no quadriceps atrophy, quadriceps MRC 5, calf muscles hypertrophy, no distal weakness ; raised CPK (HP:0003236) 4061; >61y walking (-HP:0006957)
-
-
Familial, autosomal recessive
61y
-
0y
-
-
Johan den Dunnen
00078739
0000058499
iliopsoas MRC 3.5, quadriceps atrophy, quadriceps MRC 4.5, calf muscles hypertrophy, distal weakness tibialis ant. 4/5; raised CPK (HP:0003236) 1339; >64y walking (-HP:0006957)
-
-
Isolated (sporadic)
64y
-
55y
-
-
Johan den Dunnen
00078740
0000058551
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00078792
0000058552
dystrophic muscle biopsy
-
-
Unknown
-
-
-
-
-
Tom Winder
00078793
0000058553
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00078794
0000058554
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00078795
0000058556
-
-
-
Familial
-
-
-
-
-
Tom Winder
00078797
0000058557
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Tom Winder
00078798
0000058558
-
-
-
Familial
-
-
-
-
-
Tom Winder
00078799
0000058559
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Tom Winder
00078800
0000058571
heart failure father, ambulatory with support; raised CPK (HP:0003236) 784; >69y walking (-HP:0006957)
-
-
Unknown
-
-
40y
-
-
Johan den Dunnen
00078812
0000058572
raised CPK (HP:0003236) 4387; >51y walking (-HP:0006957)
-
-
Unknown
-
-
43y
-
-
Johan den Dunnen
00078813
0000058575
dyslipidemia, CAD, ambulatory with support; raised CPK (HP:0003236) 1319; >64y walking (-HP:0006957)
-
-
Unknown
-
-
45y
-
-
Johan den Dunnen
00078816
0000058583
dyslipidemia, ECG left anterior fascicular block, ambulatory with support; raised CPK (HP:0003236) 2615; >56y walking (-HP:0006957)
-
-
Unknown
-
-
36y
-
-
Johan den Dunnen
00078824
0000058584
raised CPK (HP:0003236) 4400; >59y walking (-HP:0006957)
-
-
Unknown
-
-
43y
-
-
Johan den Dunnen
00078825
0000058586
raised CPK (HP:0003236) 1058; >45y walking (-HP:0006957)
-
-
Unknown
-
-
42y
-
-
Johan den Dunnen
00078827
0000058587
ambulatory with support; raised CPK (HP:0003236) 936; >46y walking (-HP:0006957)
-
-
Unknown
-
-
20y
-
-
Johan den Dunnen
00078828
0000058590
raised CPK (HP:0003236) 2500-4500; >52y walking (-HP:0006957)
-
-
Unknown
-
-
43y
thigh weakness/wasting
-
Johan den Dunnen
00078831
0000058591
raised CPK (HP:0003236) 686; >42y walking (-HP:0006957)
-
-
Unknown
-
-
23y
left calf wasting
-
Johan den Dunnen
00078832
0000058592
hypertrophic calves; raised CPK (HP:0003236) 784-987; >69y walking (-HP:0006957)
-
-
Unknown
-
-
40y
thigh weakness
-
Johan den Dunnen
00078833
0000058593
raised CPK (HP:0003236) 1717-3000; >55y walking (-HP:0006957)
-
-
Unknown
-
-
38y
right calf wasting
-
Johan den Dunnen
00078834
0000058594
muscle pain, axial weakness; raised CPK (HP:0003236) 1200-2200; >64y walking (-HP:0006957)
-
-
Unknown
-
-
45y
thigh weakness/wasting
-
Johan den Dunnen
00078835
0000058596
raised CPK (HP:0003236) 300-2000; >58y walking (-HP:0006957)
-
-
Unknown
-
-
<50y
raised CK
-
Johan den Dunnen
00078837
0000058597
raised CPK (HP:0003236) 1700-2900; >29y walking (-HP:0006957)
-
-
Unknown
-
-
23y
calf stiffness
-
Johan den Dunnen
00078838
0000058599
raised CPK (HP:0003236) 4200-22000; >32y walking (-HP:0006957)
-
-
Unknown
-
-
21y
reduced endurance, distal weakness
-
Johan den Dunnen
00078840
0000058602
knee hyperextension, calf pseudohypertrophy; raised CPK (HP:0003236) 2122; >63y walking (-HP:0006957)
-
-
Unknown
-
-
<60y
walking difficulties
-
Johan den Dunnen
00078843
0000058629
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Tom Winder
00078870
0000058631
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Tom Winder
00078872
0000257311
Muscle weakness (HP:0001324)
-
-
Familial, autosomal recessive
-
-
-
-
-
Ibrahim Sahin
00361913
0000292052
see paper; ..., limb-girdle weakness; no distal weakness; raised CK (2300 U/L); no exercise-induced myalgia; no rhabdomyolysis; muscle biopsy no necrosis, no regeneration, no nuclei internalization, no endomysial inflammation, no partial invasion muscle cells, no ragged-red fibers (prominent), lipid accumulation; MRI muscle thigh muscle edema, thigh muscles fatty replacement, edema of lower leg muscles, no fatty replacement of lower leg muscles
limb-girdle muscular dystrophy
-
Familial, autosomal recessive
47y
-
33y
-
-
Lidia Gonzalez-Quereda
00398963
0000295173
LGMD, myalgia
LGMW
LGMDR12-ANO5 related
Familial, autosomal recessive
32y
34y
30y
-
-
JA Bevilacqua
00402410
0000351724
Highly elevated creatine kinase Abdominal pain
LGMD
LGMDR12
Familial, autosomal recessive
-
-
-
-
-
Camille Verebi
00466360
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