Global Variome shared LOVD
B3GALNT2 (beta-1,3-N-acetylgalactosaminyltransferase 2)
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Phenotypes for disease #05329 (myalgia (myalgia))
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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/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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10 entries on 1 page. Showing entries 1 - 10.
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Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000094306
very mild, phenotype incl. cramps, myalgia, rhabdomyolisis during efforts; no intellectual disability (-HP:0001249)
myalgia
BMD
Familial, X-linked
31y
22y
-
WB DMD decreased, normal size
Human Genetics Diagnostic Laboratory - Cochin Hosp J Chelly, F Leturcq
00122778
0000099181
myalgia; upper/lower muscle weakness, difficulty walking/getting up from floor/chair; progressive weakness; no elevated serum CPK (-HP:0003236)
myalgia
-
Unknown
-
-
-
-
Johan den Dunnen
00126949
0000109647
severe muscle pain on exercise; mild calf hypertrophy; elevated serum CPK (HP:0003236) >1000
myalgia
-
Unknown
-
-
-
WB DMD reduced amount + size
Johan den Dunnen
00136898
0000109787
elevated serum CPK (HP:0003236)
myalgia
-
Unknown
-
12y
myalgia
-
Johan den Dunnen
00137038
0000163811
symptomatic carrier; calf myalgias, mild walking difficulty, distal weakness, asymmatric calf hypertrphy; CPK elevated (HP:0003236) 600-800
myalgia
-
Familial
-
65y
progressive difficulty walking, myalgias
WB and IHC DYSF reduced
Johan den Dunnen
00215359
0000164048
-
myalgia
-
Unknown
-
-
-
-
Johan den Dunnen
00215596
0000203618
-
myalgia, myoglobinuria
BMD
Unknown
22y
-
-
0.25 DMD, reduced beta-dystroglycan
Johan den Dunnen
00265832
0000318033
myalgia, muscle cramping after exercise, easy bruising; active, playing 2 sports, difficulty releasing baseball when throwing in cold; 11y-no muscle weakness, no rhabdomyolysis, no myoglobinuria, normal neurologic and physical examinations, normal development, normal developmental milestones; elevated CK (818 - 2500 U/L); 7y-muscle biopsy mild variation muscle fiber size
myalgia, muscle cramping
BMD
Familial, X-linked recessive
09y
-
-
-
Johan den Dunnen
00426895
0000318034
exercise-related myalgia and muscle cramps, fatigue; no myoglobinuria, no rhabdomyolysis, no motor delay; normal strength, abnormal attention span and hyperactivity; no calf hypertrophy, no Gower sign; elevated CK (1252 - 2722 U/L)
myalgia
-
Unknown
03y
02y
elevated liver function tests
-
Johan den Dunnen
00426896
0000344632
Rhabdomyolysis, Elevated circulating creatine kinase concentration; Metabolic myopathy, rhabdomyolysis, CK up to 50000 U/l, exercise-induced myalgia
-
-
Unknown
25y
-
-
-
Andreas Laner
00456113
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