Global Variome shared LOVD
PIGL (phosphatidylinositol glycan anchor biosynthes...)
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Curator:
Philippe Campeau
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Phenotypes for disease #00501 (SMA3 (atrophy, muscular, spinal, type III (SMA-3, juvenile, Wohlfart-Kugelberg-Welander disease)), OMIM:253400)
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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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Date
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24 entries on 1 page. Showing entries 1 - 24.
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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
0000092187
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00116708
0000092188
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Fang Song
00116709
0000092191
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00116712
0000092194
-
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00116715
0000092195
-
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00116716
0000092197
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00116718
0000092200
WB smaller SMN1
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00116721
0000092203
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00116724
0000092206
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00116727
0000092207
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00116728
0000092209
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00116730
0000092217
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00116738
0000092218
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00116739
0000092229
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00116750
0000092230
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00116751
0000092232
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00116753
0000092236
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00116757
0000092242
-
-
-
Unknown
-
-
2y6m
-
-
Johan den Dunnen
00116763
0000092251
11y-pain/heaviness in legs during exercise; later developed symptoms including waddling gait, muscle weakness and atrophy in quadriceps, attenuated patellar tendon reflex; able to walk
-
-
Familial, autosomal recessive
-
13y
11y
type 3
-
Hisahide Nishio
00116772
0000092256
13y-muscle weakness during swimming exercise; gradually lost running ability, could no longer run as fast as classmates in high school days
-
-
Isolated (sporadic)
-
-
13y
-
-
Hisahide Nishio
00116777
0000092257
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Fang Song
00116778
0000092258
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Fang Song
00116779
0000122523
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Laura Alías
00150121
0000132936
8y deterioration in specific muscle groups
-
-
Familial, autosomal recessive
-
-
03y
-
-
Kyriaki Kekou
00168074
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