Global Variome shared LOVD
CD40 (CD40 molecule, TNF receptor superfamily member 5)
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Phenotypes for disease #04242 (FRDA (Friedreich ataxia (FRDA)), OMIM:229300)
Legend
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
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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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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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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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17 entries on 1 page. Showing entries 1 - 17.
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Legend
How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000028249
8596916-Fam1
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00037733
0000028250
8596916-Fam2
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00037734
0000028251
8596916-Fam3a
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00037735
0000028252
8596917-Fam3b
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00037736
0000028253
8596918-Fam3c
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00037737
0000028255
08596916-dis
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00037739
0000028256
?
-
-
Isolated (sporadic)
24y
-
-
-
-
Nazli Basak
00037740
0000028257
08596916-Fam4
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00037741
0000028258
08596916-Fam5
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00037742
0000034304
-
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00046847
0000046786
Friedreich ataxia-like, see paper; ...,
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00060288
0000299877
-
Friedreich ataxia
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00407742
0000299878
-
Friedreich ataxia
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00407743
0000299879
-
Friedreich ataxia
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00407744
0000299929
3t-ataxia, 4y-severe cardiomyopathy
Friedreich's ataxia
FRDA
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00407801
0000299930
ataxia, scoliosis, 27y-wheelchair-bound, slow progression, signs of cardiac hypertrophy and dysarthria
Friedreich's ataxia
FRDA
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00407800
0000299931
ataxia, foot deformity, scoliosis, axonal sensory neuropathy, mild dysarthria, 15y-wheelchairbound, 21y-hypertrophic cardiomyopathy, atrophy cervical spinal cord and upper cerebellar vermis
Friedreich's ataxia
FRDA
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00407799
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