Phenotypes for disease #04255 (ALS (sclerosis, lateral, amyotrophic (ALS)))

442 entries on 5 pages. Showing entries 1 - 100.
Legend   How to query   « First ‹ Prev     1 2 3 4 5     Next › Last »

AscendingPhenotype 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
Legend   How to query   « First ‹ Prev     1 2 3 4 5     Next › Last »


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.