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Phenotypes for disease #07235 (leukodystrophy (leukodystrophy))
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.
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
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
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combination
Text
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Date
2020
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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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Date
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combination
Date
2019|2020 <2020-03
all entries in 2019 or 2020, and before March, 2020
Numeric
23
all entries exactly matching 23
|
Numeric
23|24
all entries exactly matching 23 or 24
!
Numeric
!23
all entries not exactly matching 23
<
Numeric
<23
all entries lower than 23
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Numeric
<=23
all entries lower than, or equal to, 23
>
Numeric
>23
all entries higher than 23
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Numeric
>=23
all entries higher than, or equal to, 23
combination
Numeric
>=20 <30 !23
all entries with values from 20 to 29, but not equal to 23
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Example
Matches
Asian
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Asian|African !Caucasian
all entries containing 'Asian' or 'African', but not containing 'Caucasian'
"South Asian"
all entries containing 'South Asian', but not containing 'South East Asian'
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6 entries on 1 page. Showing entries 1 - 6.
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How to query
Phenotype ID
Diagnosis/Initial
Diagnosis/Definite
Phenotype details
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Owner
Individual ID
0000357885
leukodystrophy
-
onset 18-mo with abnormal gait; Spastic gait; Flat foot; Brain MRI revealed delayed myelination or hypomyelination suggestive of Leukodystrophies; Hx of Hypothyroidism.
Unknown
2y
-
-
-
Johan den Dunnen
00473090
0000358156
leukodystrophy
-
Consanguineous parents ,sporadic case, onset 6y, lower and upper muscle weakness, foot drop , dysarthria, bulbar dysfunction, distal atrophy, gait abnormality, irritability and aggression, EDX normal report with central weakness impression , leuckodystrophy with thalamic involvement and mcp involvement reported in brain MRI
Unknown
30y
-
-
-
Johan den Dunnen
00473361
0000358163
leukodystrophy
-
bulbar dysfunction, slurred speech, ataxia, leuckodystrophy,demyelination sensorimotor polyneuropathy, scoliosis, ataxic gait, pes cavus, proximal muscle weakness and increased DTR
Unknown
37y
-
-
-
Johan den Dunnen
00473368
0000358468
leukodystrophy
-
Developmental delay, global; Low vision; Impaired chewing; Spasticity; lower limbs deformity; Difficult urination and Constipation. Brain MRI findings revealed mild to moderate ventriculomegaly and suggestive of Canavan disease and mitochondrial disorders as differential diagnosis
Familial, autosomal recessive
4y
-
-
-
Johan den Dunnen
00473673
0000358475
leukodystrophy
-
Hypotonia; Development regression; Mental retardation, severe; Strabismus; Ptosis, bilateral; No speech; Cloudy cornea; Positive history of hospitalization due to fever and leucopenia. Brain MRI showed prominence of lateral and 3th ventricles hypersignal probably due to periventricular leukoencephalopathy. Decreased serum arylsulphatase A
Unknown
6y
-
-
-
Johan den Dunnen
00473680
0000358756
leukodystrophy
-
Psychomotor regression & retardation since the age of 10-month; Hypotonia; No speech; No standing; No dysmorphic features; Mild strabismus; Small head size; Brain MRI suggestive of parenchymal volume loss, neurodegenerative disorder and leukodystrophy.
Unknown
2y
-
-
-
Johan den Dunnen
00473961
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