Global Variome shared LOVD
YES1 (v-yes-1 Yamaguchi sarcoma viral oncogene homo...)
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Phenotypes for disease #04255 (ALS (sclerosis, lateral, amyotrophic (ALS)))
Legend
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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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Text
!fs
all entries not containing 'fs'
^
Text
^p.(Arg
all entries beginning with 'p.(Arg'
$
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combination
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Date
2020
all entries matching the year 2020
|
Date
2020-03|2020-04
all entries matching March or April, 2020
!
Date
!2020-03
all entries not matching March, 2020
<
Date
<2020
all entries before the year 2020
<=
Date
<=2020-06
all entries in or before June, 2020
>
Date
>2020-06
all entries after June, 2020
>=
Date
>=2020-06-15
all entries on or after June 15th, 2020
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
Some more advanced examples:
Example
Matches
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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'
"South Asian"
all entries containing 'South Asian', but not containing 'South East Asian'
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442 entries on 5 pages. Showing entries 1 - 100.
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Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000028926
assumed dominant effect, diagnosed limb onset ALS, 63y-deceased
amyotrophic lateral sclerosis
-
Unknown
61y
-
-
-
-
Anne Polvi
00038399
0000028927
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Anne Polvi
00038400
0000028928
Assumed dominant effect
-
-
Unknown
-
-
-
-
-
Anne Polvi
00038401
0000041464
8 ALS cases
-
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00054804
0000041465
5 ALS cases
-
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00054805
0000041471
35y proximal muscle weakness, wasting upper limbs; neurological examination diffuse hyperreflexia, neurophysiological testing chronic and active denervation, motor evoked potentials demonstrated increased central conduction time both corticospinal tracts, presentation consistent with flail arm ALS variant; no evidence of cognitive impairment; developed respiratory failure, electively tracheotomised 25m after onset ALS; alive 42m after onset ALS
-
-
Unknown
-
-
35y
-
-
Johan den Dunnen
00054811
0000052929
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00073258
0000052935
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00073264
0000052943
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00073272
0000052965
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00073294
0000054323
-
-
-
Unknown
-
-
-
-
-
Simona Capponi
00074532
0000054324
-
-
-
Unknown
-
-
-
-
-
Simona Capponi
00074533
0000054373
Progressive proximal muscle weakness in upper extremities (HP:0009073), atrophy (HP:?), fasciculation in the left proximal upper arm and hand (HP:0007289), reduced Tendon reflexes (HP:0001315), no Hoffmann sign (-HP:?), no Babinski signs (-HP:0003487), no paraspinal muscle reflex (-HP:?), fasciculations (HP:0002380), serious respiratory disability (HP:0002880)
-
-
Familial, autosomal dominant
-
-
35y
progressive weakness of the left forefinger (HP:?)
-
Jamie Zeegers
00074617
0000054375
weakness in the right lower extremity (HP:?), atrophy in the right lower limb (HP:?), fasciculation in all 4 extremities (HP:0002380), Hoffmann sign (HP:?), Babinski signs (HP:0003487), paraspinal muscle reflex (HP:?), neurogenic damage of the cervical, thoracic, and lumbar segments (HP:?),
-
-
Familial, autosomal dominant
-
-
-
-
-
Jamie Zeegers
00074619
0000054376
difficulty in walking (HP:0002355), weakness of lower limbs (HP:0007340), fasciculations of lower limbs (HP:0007289), difficulty in rising from lying to sitting position (HP:?), slight slurring of speech (HP:0002465), breathlessness while speaking (HP:?), atrophy and weakness of distal muscles of lower limbs(HP:0002460), weakness of proximal muscles (HP:0003701), mild weakness of trunk muscles (HP:?), jaw jerk (HP:?), palmomental reflex (HP:0002476), exaggerated tendon reflexes (HP:0006801), standing with support (HP:0003698), active denervation in bulbar area and muscles of both lower limbs (HP:?),
-
-
Familial, autosomal dominant
-
-
-
-
-
Jamie Zeegers
00074620
0000054378
weakness of the left hand (HP:?), widespread fasciculations (HP:0002380), slurring of speech (HP:0002465), no swallowing difficulties (-HP:0002015), no breathlessness (-HP:?), no impairment of memory (-HP:0002354), no emotional lability (-HP:0000712), no difficulty walking (-HP:0002355), no difficulty climbing stairs (-HP:0003551), atrophy (HP:?), weakness of interossei, thenar and hypothenar muscles of the left hand (HP:?), moderate weakness of trunk muscles (HP:?), power in the lower limbs was normal (HP:?), exaggerated deep tendon reflexes (HP:0006801), plantars were extensor (HP:?), acute and chronic denervation (HP:?), reinnervation (HP:?),
-
-
Familial, autosomal dominant
-
-
-
-
-
Jamie Zeegers
00074622
0000054381
dysarthria (HP:0001260), weakness in her left proximal arm (HP:0003701), respiratory difficulty with dysphagia (HP:0002015), no cognitive and/or behavioral impairments (-HP:0100543)
-
-
Isolated (sporadic)
-
-
27y
-
-
Jamie Zeegers
00074626
0000054383
weakness in her right distal arm (HP:0002460), dysarthria (HP:0001260), respiratory difficulty (HP:?), no cognitive and/or behavioral impairments (-HP:0100543)
-
-
Isolated (sporadic)
-
-
31y
-
-
Jamie Zeegers
00074627
0000054407
difficulty walking (HP:0002355), lower motor neuron signs (HP:0002366), upper motor neuron signs (HP:?), no bulbar signs (-HP:0002483), active denervation (HP:?), dysarthria (HP:0001260), choking (HP:?), no denutrition (-HP:?), no respiratory insufficiency (-HP:0002093)
-
-
Isolated (sporadic)
-
-
-
-
-
Jamie Zeegers
00074655
0000054410
mild muscle weakness in both lower extremities (HP:0003484), muscle pain (HP:0003326), fasciculation (HP:0002380), weakness and wasting in the proximal muscles of both lower extremities (HP:0008994), difficulty walking (HP:0002355), no cognitive impairment (-HP:0100543), bulbar palsy (HP:0001283), Brisk tendon reflexes (HP:0006801), no Babinski signs (-HP:0003487)
-
-
Isolated (sporadic)
-
-
-
-
-
Jamie Zeegers
00074657
0000058302
dysphagia (HP:0002015), progressive muscle weakness (HP:0003323), atrophy in upper and lower limbs (HP:?), feeding problems (HP:0011968), increased jaw jerk (HP:?), hyperactive gag reflexes (HP:?), generalized atrophy (HP:0003700), severe weakness of four limbs (HP:0002273), severe weakness neck muscles (HP:0000467) with fasciculations (HP:0002380), brisk deep tendon reflexes (HP:0006801), with extensor plantar responses (HP:0003487), aspiration pneumonia (HP:0011951), respiratory failure (HP:0002878)
-
-
Isolated (sporadic)
56y
-
53y
Bulbar (HP:0002483), slurred speech (HP:0001350)
-
Jamie Zeegers
00078526
0000058303
abnormal upper motor neuron involvement (HP:0002493), normal lower motor neuron involvement (-HP:0002366), bulbar palsy (HP:0001283), no respiratory failure (-HP:0002878)
-
-
Familial, autosomal dominant
-
-
74y
-
-
Jamie Zeegers
00078527
0000058304
normal lower motor neuron involvement (-HP:0002366)
-
-
Familial, autosomal dominant
-
-
73y
-
-
Jamie Zeegers
00078528
0000058305
no abnormal upper motor neuron involvement (-HP:0002493), normal lower motor neuron involvement (-HP:0002366), bulbar palsy (HP:0001283), no respiratory failure (-HP:0002878)
-
-
Familial, autosomal dominant
-
-
68y
-
-
Jamie Zeegers
00078529
0000058306
normal lower motor neuron involvement (-HP:0002366), bulbar palsy (HP:0001283), respiratory failure (HP:0002878)
-
-
Familial, autosomal dominant
-
-
53y
-
-
Jamie Zeegers
00078530
0000058307
progressive limbs weakness (HP:0002273), gait impairment (HP:0001288), proximal muscle weakness (HP:0003701), widespread fasciculations (HP:0002380), limb hypertonia (HP:0002509), bulbar signs (HP:0002483), no cognitive or behavioural disturbances (-HP:0100543), mild mood depression (HP:0000716)
-
-
Familial, autosomal dominant
-
-
45y
-
-
Jamie Zeegers
00078531
0000058308
progressive limb weakness (HP:0003690)
-
-
Familial, autosomal dominant
-
-
60y
-
-
Jamie Zeegers
00078532
0000058309
progressive lower leg weakness (HP:0007340), spasticity (HP:0001257)
-
-
Familial, autosomal dominant
-
-
30y
-
-
Jamie Zeegers
00078533
0000058310
slowly progressive limb weakness (HP:0003690)
-
-
Familial, autosomal dominant
-
-
47y
-
-
Jamie Zeegers
00078534
0000058311
pancytopenia (HP:0001876), leg pain (HP:?), nonitching rash on the right lower leg (HP:?), mild respiratory symptoms including runny nose and sneezing(HP:?), red-colored urine (HP:?), splenomegaly (HP:0001744), petechiae (HP:0000967), pancytopenia (HP:0001876), scaling eczemas (HP:0000964), proteinuria (HP:0000093),
-
-
Familial, autosomal recessive
-
-
01y
bilateral orchidopexy (HP:?), idiopathic facial nerve palsy (HP:0010628), mycosis pedis (HP:?), pollinosis (HP:?)
-
Jamie Zeegers
00078535
0000058312
upper motor neuron involvement (HP:0002493), no cognitive involvement (-HP:0100543)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00078536
0000058313
upper motor neuron involvement (HP:0002493), no cognitive involvement (-HP:0100543)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00078537
0000058314
rapidly progressive presenile dementia (HP:0000726), motor neuron damage (HP:0002493)
-
-
Familial, autosomal recessive
-
-
-
-
-
Jamie Zeegers
00078538
0000058319
atrophy of the tongue (HP:0012473), dysphagia (HP:0002015), dyspnea (HP:0002094), diffuse muscle atrophies (HP:0003700), fasciculations of the 4 arms/neck/dorsal muscles (HP:0002380), moderate weakness of all limb muscles (HP:0009028), moderate weakness of the flexor and extensor muscles of the neck (HP:?), brisk deep tendon reflexes (HP:0006801), bilaterally plantar response (HP:?)
-
-
Isolated (sporadic)
-
-
72y
progressive weakness of the right hand (HP:0003323), atrophy of the right hand (HP:0009130)
-
Jamie Zeegers
00078543
0000058320
muscle weakness extended to all 4 limbs (HP:0003690), bulbar signs (HP:0002483), severe amyotrophy of all 4 limbs (HP:0003202), diminished deep tendon reflexes (HP:0001265), extensor plantar reflexes (HP:0003487), tongue atrophic (HP:0012473), complete tetraparesis (HP:0002273), hearing difficulty (HP:?), mental impairment ( HP:0100543), complete limb palsy (HP:?), atrophy of the frontal and temporal lobes (HP:0006892), dementia (HP:0000726)
-
-
Isolated (sporadic)
-
-
62y
spondylotic myelopathy (HP:0002318)
-
Jamie Zeegers
00078544
0000092645
amyotrophic lateral sclerosis
-
-
Familial
-
-
-
-
-
Ariel I Suarez
00117410
0000106787
see paper; ...
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00134037
0000116445
increased deep tendon reflexes in the lower limbs (HP:0002395), hand interosseous muscle atrophy (HP:0007181), limb fasciculation (HP:0007289) and muscle fibrillation (HP:0010546)in right first interracial, biceps and both tibialis anterior muscles, tongue fasciculations (HP:0001308)
-
-
Familial, autosomal recessive
25y
20y?
15y-20y
Difficulty in walking (HP:0002355)
-
Ceren Tunca
00143683
0000116559
-
-
-
Familial, autosomal recessive
37y
37y
32y
-
-
Ceren Tunca
00143789
0000116560
-
-
-
Familial, autosomal recessive
53y
53y
49y
-
-
Ceren Tunca
00143791
0000116561
-
-
-
Familial, autosomal recessive
15y
15y
15y?
-
-
Ceren Tunca
00143792
0000119796
no dementia, no Paget’s disease of bone
amyotrophic lateral sclerosis
-
Isolated (sporadic)
-
-
58y
limb
-
Johan den Dunnen
00147080
0000119797
no dementia, no Paget’s disease of bone
amyotrophic lateral sclerosis
-
Isolated (sporadic)
-
-
39y
limb
-
Johan den Dunnen
00147081
0000119798
no dementia, no Paget’s disease of bone
amyotrophic lateral sclerosis
-
Isolated (sporadic)
-
-
59y
limb
-
Johan den Dunnen
00147082
0000119799
no dementia, no Paget’s disease of bone
amyotrophic lateral sclerosis
-
Isolated (sporadic)
-
-
38y
limb
-
Johan den Dunnen
00147083
0000119800
no dementia, no Paget’s disease of bone
amyotrophic lateral sclerosis
-
Isolated (sporadic)
-
-
65y
limb
-
Johan den Dunnen
00147084
0000119801
no dementia, no Paget’s disease of bone
amyotrophic lateral sclerosis
-
Isolated (sporadic)
-
-
38y
limb
-
Johan den Dunnen
00147085
0000125664
atrophy inarms, hands, distal lower extremities, paravertebral muscles, asymmetric tetraparesis, diminished tendon reflexes, unresponsive plantar reflexes; 20y lost ambulation
sclerosis, lateral, amyotrophic
-
Familial, autosomal recessive
47y
-
31y
-
-
Johan den Dunnen
00152721
0000125665
atrophy in arms and distal lower extremities and paravertebral muscles, asymmetric weakness all extremities, brisk tendon reflexes, bilateral Wartenberg sign, left Babinski sign, fasciculations, bulbar symptoms (uvula deviation to right and left palatal arch weakness); 44y-ambulant
-
-
Familial, autosomal recessive
44y
-
35y
-
-
Johan den Dunnen
00152722
0000125666
asymmetric weakness in legs, atrophy paravertebral and distal lower extremity muscles, brisk tendon reflexes, unresponsive plantar reflexes; 27y-ambulant
-
-
Familial, autosomal recessive
37y
-
27y
-
-
Johan den Dunnen
00152723
0000125667
atrophy in all limbs and paravertebral muscles, asymmetric weakness forearms and lower extremities; 17y-lost ambulation
-
-
Familial, autosomal recessive
43y
-
27y
-
-
Johan den Dunnen
00152724
0000125668
severe atrophy in lower extremities and paravertebral muscles, generalized weakness, unresponsive plantar reflexes, diminished tendon reflexes, high arch feet, hammer toe; never walked
-
-
Familial, autosomal recessive
28y
-
12y
-
-
Johan den Dunnen
00152725
0000152887
-
-
-
Isolated (sporadic)
-
-
56y
-
-
Serena Lattante
00204650
0000152888
-
-
-
Isolated (sporadic)
-
-
27y
-
-
Serena Lattante
00204651
0000152889
-
-
-
Isolated (sporadic)
-
-
48y
-
-
Serena Lattante
00204652
0000152890
-
-
-
Isolated (sporadic)
-
-
66y
-
-
Serena Lattante
00204653
0000152891
-
-
-
Isolated (sporadic)
-
-
52y
-
-
Serena Lattante
00204654
0000152892
-
-
-
Isolated (sporadic)
-
-
65y
-
-
Serena Lattante
00204655
0000152893
-
-
-
Isolated (sporadic)
-
-
70y
-
-
Serena Lattante
00204656
0000152894
-
-
-
Familial
-
-
47y
-
-
Serena Lattante
00204657
0000152895
-
-
-
Isolated (sporadic)
-
-
53y
-
-
Serena Lattante
00204658
0000152896
-
-
-
Familial
-
-
67y
-
-
Serena Lattante
00204659
0000152897
-
-
-
Isolated (sporadic)
-
-
59y
-
-
Serena Lattante
00204660
0000152898
-
-
-
Isolated (sporadic)
-
-
65y
-
-
Serena Lattante
00204661
0000152899
-
-
-
Isolated (sporadic)
-
-
62y
-
-
Serena Lattante
00204662
0000152900
-
-
-
Familial
-
-
77y
-
-
Serena Lattante
00204663
0000152901
-
-
-
Isolated (sporadic)
-
-
73y
-
-
Serena Lattante
00204664
0000152902
-
-
-
Familial
-
-
66y
-
-
Serena Lattante
00204665
0000152903
-
-
-
Familial
-
-
63y
-
-
Serena Lattante
00204666
0000152904
-
-
-
Isolated (sporadic)
-
-
48y
-
-
Serena Lattante
00204667
0000152905
-
-
-
Isolated (sporadic)
-
-
68y
-
-
Serena Lattante
00204668
0000152906
-
-
-
Isolated (sporadic)
-
-
49y
-
-
Serena Lattante
00204669
0000152907
-
-
-
Familial
-
-
62y
-
-
Serena Lattante
00204670
0000152908
-
-
-
Familial
-
-
57y
-
-
Serena Lattante
00204671
0000152909
-
-
-
Isolated (sporadic)
-
-
52y
-
-
Serena Lattante
00204672
0000152910
-
-
-
Isolated (sporadic)
-
-
54y
-
-
Serena Lattante
00204673
0000152911
-
-
-
Isolated (sporadic)
-
-
64y
-
-
Serena Lattante
00204674
0000152912
-
-
-
Isolated (sporadic)
-
-
37y
-
-
Serena Lattante
00204675
0000152913
-
-
-
Isolated (sporadic)
-
-
52y
-
-
Serena Lattante
00204676
0000152914
-
-
-
Familial
-
-
80y
-
-
Serena Lattante
00204677
0000152915
-
-
-
Familial
-
-
52y
-
-
Serena Lattante
00204678
0000152916
-
-
-
Familial
-
-
52y
-
-
Serena Lattante
00204679
0000152917
-
-
-
Isolated (sporadic)
-
-
53y
-
-
Serena Lattante
00204680
0000152918
-
-
-
Familial
-
-
50y
-
-
Serena Lattante
00204681
0000152919
-
-
-
Familial
-
-
?
-
-
Serena Lattante
00204682
0000152920
-
-
-
Familial
-
-
83y
-
-
Serena Lattante
00204683
0000152921
-
-
-
Familial
-
-
74y
-
-
Serena Lattante
00204684
0000152922
-
-
-
Familial
-
-
63y
-
-
Serena Lattante
00204685
0000152923
-
-
-
Isolated (sporadic)
-
-
53y
-
-
Serena Lattante
00204686
0000152924
-
-
-
Isolated (sporadic)
-
-
38y
-
-
Serena Lattante
00204687
0000152925
-
-
-
Isolated (sporadic)
-
-
72y
-
-
Serena Lattante
00204688
0000152926
-
-
-
Familial
-
-
64y
-
-
Serena Lattante
00204689
0000152927
-
-
-
Isolated (sporadic)
-
-
20y
-
-
Serena Lattante
00204690
0000152928
-
-
-
Familial
-
-
57y
-
-
Serena Lattante
00204691
0000152929
-
-
-
Familial
-
-
47y
-
-
Serena Lattante
00204692
0000152930
-
-
-
Familial
-
-
57y
-
-
Serena Lattante
00204693
0000152931
-
-
-
Familial
-
-
53y
-
-
Serena Lattante
00204694
0000152932
-
-
-
Familial
-
-
61y
-
-
Serena Lattante
00204695
0000152933
-
-
-
Familial
-
-
47y
-
-
Serena Lattante
00204696
0000152934
-
-
-
Familial
-
-
38y
-
-
Serena Lattante
00204697
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