Global Variome shared LOVD
RAD50 (RAD50 homolog (S. cerevisiae))
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Phenotypes for disease #01944 (LGMDR5;LGMD2C (dystrophy, muscular, limb-girdle, autosomal recessive, type 5 (LGMD2C)), OMIM:253700)
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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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20 entries on 1 page. Showing entries 1 - 20.
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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
0000051911
proximal muscle weakness (HP:0003701), no motor delay (-HP:0001270), no cognitive impairment (-HP:0100543), no ambulation (-HP:0002540), bilateral calf hypertrophy (HP:0008981), mild scapular winging (HP:0003691), no joint contractures (-HP:0001371)
-
-
Familial, autosomal recessive
-
-
06y
-
-
Jamie Zeegers
00072206
0000051912
proximal muscle weakness (HP:0003701), no ambulation (-HP:0002540), bilateral calf hypertrophy (HP:0008981), mild scapular winging (HP:0003691), no joint contractures (-HP:0001371), pelvic girdle muscles weakness (HP:0003749), lordosis (HP:0003307), waddling gait (HP:0002515), macroglossia (HP:0000158), no facial weakness (-HP:0010628)
-
-
Familial, autosomal recessive
-
-
09y
-
-
Jamie Zeegers
00072208
0000106030
clinical grade V; elevated CPK (HP:0003236); >17y-inable to walk (HP:0002540)
severe autosomal recessive muscular dystrophy, North African type (SCARMD)
-
Isolated (sporadic)
-
7y
7y
difficulty climbing stairs/running
IHC/WB SGCA trace
Johan den Dunnen
00133283
0000106045
clinical grade VI/VII; 21y-inable to walk (HP:0002540)
severe autosomal recessive muscular dystrophy, North African type (SCARMD)
-
Isolated (sporadic)
-
8y
8y
difficulty climbing stairs/running
IHC SGCA trace, SGC weak, SSPN weak; WB SGCA trace
Johan den Dunnen
00133298
0000106046
clinical grade III; >26y-inable to walk (HP:0002540)
severe autosomal recessive muscular dystrophy, North African type (SCARMD)
-
Isolated (sporadic)
-
12y
14y
difficulty climbing stairs/running
IHC/WB SGCA weak; IHC SGC weak, SSPN weak
Johan den Dunnen
00133299
0000106048
13y-inable to walk (HP:0002540)
severe autosomal recessive muscular dystrophy, North African type (SCARMD)
-
Isolated (sporadic)
-
9y
-
-
-
Johan den Dunnen
00133301
0000106056
severe (clinical grade VII), walk tip-toe; 22y-inable to walk (HP:0002540)
severe autosomal recessive muscular dystrophy, North African type (SCARMD)
-
Isolated (sporadic)
-
9y
6y
difficulty climbing stairs/running
IHC/WB no SGCA
Johan den Dunnen
00133309
0000106100
clinical grade IV, walk tip-toe; >36y-inable to walk (HP:0002540)
severe autosomal recessive muscular dystrophy, North African type (SCARMD)
-
Isolated (sporadic)
-
9y
6y
difficulty climbing stairs/running
IHC/WB SGCA weak
Johan den Dunnen
00133353
0000106113
-
severe autosomal recessive muscular dystrophy, North African type (SCARMD)
-
Isolated (sporadic)
-
-
-
-
IHC SGC weak, SSPN weak
Johan den Dunnen
00133366
0000106117
severe; 22y-inable to walk (HP:0002540)/10y-inable to walk (HP:0002540)-
severe autosomal recessive muscular dystrophy, North African type (SCARMD)
-
Isolated (sporadic)
-
07y-09y
-
-
-
Johan den Dunnen
00133370
0000106120
clinical grade III; >25y-inable to walk (HP:0002540)
severe autosomal recessive muscular dystrophy, North African type (SCARMD)
-
Isolated (sporadic)
-
12y
13y
difficulty climbing stairs/running
IHC SGCA weak, WB SGCA trace
Johan den Dunnen
00133373
0000106133
1108 elevated CPK (HP:0003236)
severe autosomal recessive muscular dystrophy, North African type (SCARMD)
-
Unknown
-
-
15y
-
-
Johan den Dunnen
00133386
0000106134
clinical grade III; >31y-inable to walk (HP:0002540)
severe autosomal recessive muscular dystrophy, North African type (SCARMD)
-
Familial
-
15y
-
exercise intolerance
IHC SGC weak, SSPN weak
Johan den Dunnen
00133387
0000106135
clinical grade III; >33y-inable to walk (HP:0002540)
severe autosomal recessive muscular dystrophy, North African type (SCARMD)
-
Familial
-
12y
-
exercise intolerance
IHC SGCA weak, WB SGCA reduced
Johan den Dunnen
00133388
0000106138
severe (clinical grade VII), walk tip-toe; 14y-inable to walk (HP:0002540)
severe autosomal recessive muscular dystrophy, North African type (SCARMD)
-
Isolated (sporadic)
-
6y
6y
difficulty climbing stairs/running
IHC no SGCA, WB SGCA trace
Johan den Dunnen
00133391
0000106219
severe (clinical grade VII), walk tip-toe; 13y-inable to walk (HP:0002540)
severe autosomal recessive muscular dystrophy, North African type (SCARMD)
-
Isolated (sporadic)
-
6y
6y
difficulty climbing stairs/running
IHC no SGCA, IHC SGC weak, SSPN weak; WB SGCA trace
Johan den Dunnen
00133472
0000106258
-
severe autosomal recessive muscular dystrophy, North African type (SCARMD)
-
Familial
-
-
-
-
-
Marina Fanin
00133511
0000106260
-
severe autosomal recessive muscular dystrophy, North African type (SCARMD)
-
Unknown
-
-
-
-
WB reduced SGCA
Marina Fanin
00133513
0000161574
Suspected Duchenne muscular dystrophy, but with normal results on multiplex PCR and MLPA for DMD gene
Suspected Duchenne muscular dystrophy
Limb-girdle muscular dystrophy type 2C (LGMD2C)
Familial, autosomal recessive
08y
-
?
Muscular dystrophy
No muscle biopsy performed
Miguel Angel Alcántara-Ortigoza
00213094
0000322150
Elevated circulating creatine kinase concentration, Muscle atrophy
-
-
Familial, autosomal recessive
06y
-
-
-
-
Andreas Laner
00431575
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