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Phenotypes for disease #02143 (ALD (adrenoleukodystrophy (ALD)), OMIM:300100)
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
Intellectual_dis
: individual has intellectual disability (intellectual disability (mental retardation), HP:0001249,mental retardation); please specify
All options:
yes = intellectual disability (HP:0001249, IQ below 70)
borderline = intellectual disability, borderline (HP:0006889, IQ 70-79)
mild = intellectual disability, mild (HP:0001256, IQ 50-69)
moderate = intellectual disability, moderate (HP:0002342, IQ 35-49)
profound = intellectual disability, profound (HP:0002187, IQ below 20)
severe = intellectual disability, severe (HP:0010864, IQ 20-34)
progressive = intellectual disability, progressive (HP:0006887)
no = no intellectual disability (IQ above 79, -)
? = unknown
n/a = not analysed
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43 entries on 1 page. Showing entries 1 - 43.
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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
Intellectual_dis
Owner
Individual ID
0000038756
born 40w gestation, birth weight 3198g; 1y-normal developmental milestones; walk-12m; 3y-speak two-word sentences; developed convulsions several times since age 2y; 39m-admitted to hospital, normal height/weight/physical examinations, ECG spikes and spike-and-waves left occicipital region; MRI brain FLAIR-method high signal intensity areas both occicipital regions, small high-signal-intensity areas scattered in anterior/temporal parts cerebrum; motor and sensory nerve conduction velocity normal; ...
-
-
Isolated (sporadic)
-
-
-
-
-
-
Johan den Dunnen
00052135
0000038924
adolescent adrenoleukodystrophy (AALD); increased levels of very long chain fatty acids (VLCFA)
-
-
Familial, X-linked dominant
29y
-
-
-
-
-
Johan den Dunnen
00052348
0000038925
childhood cerebral adrenoleukodystrophy (CALD), died after clinical course of 4y; increased levels of very long chain fatty acids (VLCFA)
-
-
Familial, X-linked dominant
-
-
09y
-
-
-
Johan den Dunnen
00052349
0000038926
childhood cerebral adrenoleukodystrophy (CALD), died after clinical course of 1.5y; increased levels of very long chain fatty acids (VLCFA)
-
-
Familial, X-linked dominant
-
-
07y
-
-
-
Johan den Dunnen
00052350
0000038928
boy died of childhood cerebral ALD (CCALD)
-
-
Familial, X-linked
-
-
-
-
-
-
Johan den Dunnen
00052352
0000038929
adrenomyeloneuropathy (AMN)
-
-
Familial, X-linked
-
-
-
-
-
-
Johan den Dunnen
00052353
0000038930
both patients have adrenomyeloneuropathy (AMN)
-
-
Familial, X-linked
-
-
-
-
-
-
Johan den Dunnen
00052354
0000038931
childhood cerebral ALD (CCALD) and young symptomatic
-
-
Familial, X-linked
-
-
-
-
-
-
Johan den Dunnen
00052355
0000038932
both patients have adrenomyeloneuropathy (AMN)
-
-
Familial, X-linked
-
-
-
-
-
-
Johan den Dunnen
00052356
0000038952
childhood cerebral adrenoleukodystrophy (CALD); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052378
0000038953
childhood cerebral adrenoleukodystrophy (CALD); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052379
0000038954
increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052380
0000038955
increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052381
0000038956
childhood cerebral adrenoleukodystrophy (CALD); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052382
0000038957
childhood cerebral adrenoleukodystrophy (CALD); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052383
0000038958
adrenomyeloneuropathy (AMN); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052384
0000038959
adrenomyeloneuropathy (AMN); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052385
0000038960
adrenomyeloneuropathy (AMN); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052386
0000038961
childhood cerebral adrenoleukodystrophy (CALD); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052387
0000038962
adrenomyeloneuropathy (AMN); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052388
0000038963
childhood cerebral adrenoleukodystrophy (CALD); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052389
0000038964
adrenomyeloneuropathy (AMN); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052390
0000038965
symptomatic carrier; increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052391
0000038966
childhood cerebral adrenoleukodystrophy (CALD); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052392
0000038967
increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052393
0000038968
adrenomyeloneuropathy (AMN); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052394
0000038969
adrenomyeloneuropathy (AMN); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052395
0000038970
adrenomyeloneuropathy (AMN); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052396
0000038971
adrenomyeloneuropathy (AMN); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052397
0000038972
adrenomyeloneuropathy (AMN); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052398
0000038973
childhood cerebral adrenoleukodystrophy (CALD); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052399
0000038974
childhood cerebral adrenoleukodystrophy (CALD); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052400
0000038975
adrenomyeloneuropathy (AMN); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052401
0000038976
increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052402
0000038977
childhood cerebral adrenoleukodystrophy (CALD); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052403
0000038978
childhood cerebral adrenoleukodystrophy (CALD); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052404
0000038979
childhood cerebral adrenoleukodystrophy (CALD); increased levels of very long chain fatty acids (VLCFA)
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00052405
0000038985
childhood cerebral adrenoleukodystrophy (CCALD), hyperpigmentation; VLCFA 5.6 (<0.89), ACTH 221 (1-10); MRI-dilation cerebral ventricles
-
-
Familial, X-linked
-
04y06m
01y
-
-
no
Johan den Dunnen
00052408
0000038986
Addison only (AO), hematopoietic stem cell transplantation, hyperpigmentation; VLCFA 5.84 (<0.89), ACTH 110 (1-10); MRI-no white matter lesions
-
-
Familial, X-linked
-
02y03m
01y03m
-
-
no
Johan den Dunnen
00052409
0000274619
Neuroregression; hearing problems; adrenal insufficiency (Neurology)
-
Adrenoleukodystrophy
Familial
-
-
-
-
-
-
LOVD
00380766
0000308913
-
-
-
Familial, X-linked recessive
-
-
-
-
-
-
Wenjuan Qiu
00417427
0000310379
Increased circulating very long-chain fatty acid concentration (HP:0033643); Demyelination in central white matter(HP:0007305)
ALD
ALD
Familial, X-linked
06y07m
06y09m
?
no symptom
-
no
Feixia Zheng
00419090
0000347701
see paper; ..., severe hypotonia, intellectual disability, seizures, no dysmorphic features; enlarged hepatic peroxisomes
adrenoleukodystrophy
peroxisomal acyl-CoA oxidase deficiency
Familial, autosomal recessive
-
-
-
-
-
-
Johan den Dunnen
00459974
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