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Phenotypes for disease #00197 (SPG17 (paraplegia, spastic, autosomal dominant, type 17 (SPG-17, Silver)), OMIM:270685)
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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/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
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
Phenotype/Onset
: individual's phenotype at Age/Onset described using HPO
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
Protein
: result from protein staining
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all entries containing 'Arg'
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Text
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all entries not containing 'fs'
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Text
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all entries beginning with 'p.(Arg'
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all entries ending with 'Ser)'
=""
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Text
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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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all entries before the year 2020
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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
combination
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
|
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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all entries higher than 23
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Numeric
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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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33 entries on 1 page. Showing entries 1 - 33.
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How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Onset
Age/Diagnosis
Phenotype/Onset
Age/Examination
Protein
Owner
Individual ID
0000001688
Silver syndrome; spastic paraparesis, amyotrophy hands
-
-
Familial, autosomal dominant
-
-
-
-
-
María-Jesús Sobrido
00002774
0000001689
Silver syndrome; spastic paraparesis, amyotrophy hands
-
-
Familial, autosomal dominant
-
-
-
-
-
María-Jesús Sobrido
00002775
0000001690
Silver syndrome; spastic paraparesis, amyotrophy hands
-
-
Familial, autosomal dominant
-
-
-
-
-
María-Jesús Sobrido
00002776
0000001691
Silver syndrome; spastic paraparesis, amyotrophy hands
-
-
Familial, autosomal dominant
-
-
-
-
-
María-Jesús Sobrido
00002777
0000001692
Silver syndrome; spastic paraparesis, with distal amyotrophy always starting and predominating in legs
-
-
Familial, autosomal dominant
-
-
-
-
-
María-Jesús Sobrido
00002778
0000001693
Silver syndrome;
-
-
Familial, autosomal dominant
-
-
-
-
-
María-Jesús Sobrido
00002779
0000001694
Silver syndrome;
-
-
Familial, autosomal dominant
-
-
-
-
-
María-Jesús Sobrido
00002780
0000001710
Silver syndrome; hereditary motor neuropathy, distal (dHMN)
-
-
Familial, autosomal dominant
-
-
-
-
-
María-Jesús Sobrido
00002796
0000001711
Silver syndrome; hereditary motor neuropathy, distal (dHMN)
-
-
Familial, autosomal dominant
-
-
-
-
-
María-Jesús Sobrido
00002797
0000001714
Silver syndrome; hereditary motor neuropathy, distal (dHMN)
-
-
Familial, autosomal dominant
-
-
-
-
-
María-Jesús Sobrido
00002800
0000001715
Silver syndrome; hereditary motor neuropathy, distal (dHMN); retained/brisk reflexes
-
-
Unknown
-
-
-
-
-
María-Jesús Sobrido
00002801
0000001718
Silver syndrome;
-
-
Familial, autosomal dominant
-
-
-
-
-
María-Jesús Sobrido
00002804
0000001719
Silver syndrome;
-
-
Isolated (sporadic)
-
-
-
-
-
María-Jesús Sobrido
00002805
0000001746
spastic paraplegia (SP); early onset; complicated form: spinal and cerebellar signs
-
-
Isolated (sporadic)
-
-
-
-
-
María-Jesús Sobrido
00002832
0000001749
spastic paraplegia (SP); late onset, pure SP
-
-
Familial, autosomal dominant
-
-
-
-
-
María-Jesús Sobrido
00002835
0000001751
spastic paraplegia (SP); early-onset SP
-
-
Isolated (sporadic)
-
-
-
-
-
María-Jesús Sobrido
00002837
0000001754
spastic paraplegia (SP); early-onset SP
-
-
Isolated (sporadic)
-
-
-
-
-
María-Jesús Sobrido
00002840
0000001756
spastic paraplegia (SP); late-onset, pure SP
-
-
Isolated (sporadic)
-
-
-
-
-
María-Jesús Sobrido
00002842
0000001757
SP; SS; dHMN; variability among patients: pure SP, SS, dHMN or subclinical signs
-
-
Familial
-
-
-
-
-
María-Jesús Sobrido
00002843
0000001759
spastic paraplegia (SP); Silver Syndrome (SS); CMT2; variability among patients, all spectrum of phenotype: pure SP, SS, CMT2
-
-
Familial
-
-
-
-
-
María-Jesús Sobrido
00002845
0000001762
spastic paraplegia (SP); early -onset, complicated SP, mild MR, thin corpus callosum
-
-
Isolated (sporadic)
-
-
-
-
-
María-Jesús Sobrido
00002848
0000001763
spastic paraplegia (SP); young-onset SP, complicated form: pyramidal signs, sensory involvement (proprioceptive >tactile/pain), gait ataxia
-
-
Unknown
-
-
-
-
-
María-Jesús Sobrido
00002849
0000001764
spastic paraplegia (SP); early-onset SP, complicated form: pyramidal signs, MR, visual impairment
-
-
Isolated (sporadic)
-
-
-
-
-
María-Jesús Sobrido
00002850
0000001766
spastic paraplegia (SP); SP, no other clinical data available
-
-
Unknown
-
-
-
-
-
María-Jesús Sobrido
00002852
0000001767
spastic paraplegia (SP); early-onset, pure SP
-
-
Isolated (sporadic)
-
-
-
-
-
María-Jesús Sobrido
00002853
0000001770
Silver syndrome
-
-
Familial, autosomal dominant
-
-
-
-
-
María-Jesús Sobrido
00002856
0000001774
Silver syndrome
-
-
Familial, autosomal dominant
-
-
-
-
-
María-Jesús Sobrido
00002860
0000001778
Silver syndrome
-
-
Familial, autosomal dominant
-
-
-
-
-
María-Jesús Sobrido
00002864
0000001779
Silver syndrome
-
-
Familial, autosomal dominant
-
-
-
-
-
María-Jesús Sobrido
00002865
0000001780
Silver syndrome
-
-
Familial, autosomal dominant
-
-
-
-
-
María-Jesús Sobrido
00002866
0000001781
Silver syndrome
-
-
Isolated (sporadic)
-
-
-
-
-
María-Jesús Sobrido
00002867
0000001812
Silver syndrome
-
-
Familial, autosomal dominant
-
-
-
-
-
María-Jesús Sobrido
00002898
0000001815
SS, dHMN, Asymptomatic
-
-
Familial, autosomal dominant
-
-
-
-
-
María-Jesús Sobrido
00002901
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