Babinski sign
Symptom Information:
Symptom ID: | HPO:0003487 | ||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of central motor function(HPO:0011442) Abnormal pyramidal signs(HPO:0007256) Babinski sign(HPO:0003487) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Abnormal reflexes(MedDRA:10000171) Babinski sign(HPO:0003487) |
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Database Frequency: | 179 / 7739 | ||||||||||||||||
Resource: |
All diseases associated with this symptom:
3-methylglutaconic aciduria type 3 | (Orphanet:67047) |
ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME | (OMIM:231550) |
ALZHEIMER DISEASE 3 | (OMIM:607822) |
AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA | (OMIM:612069) |
AMYOTROPHIC LATERAL SCLEROSIS 17 | (OMIM:614696) |
AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE | (OMIM:205100) |
AMYOTROPHIC LATERAL SCLEROSIS 5 | (OMIM:602099) |
ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS ANDDIABETES MELLITUS | (OMIM:616192) |
ATAXIA, SENSORY, 1, AUTOSOMAL DOMINANT | (OMIM:608984) |
ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTICATROPHY AND MENTAL RETARDATION | (OMIM:270500) |
Adult polyglucosan body disease | (Orphanet:206583) |
Adult-onset autosomal dominant leukodystrophy | (Orphanet:99027) |
Allan-Herndon-Dudley syndrome | (Orphanet:59) |
Alpha-mannosidosis | (Orphanet:61) |
Amyotrophic lateral sclerosis type 4 | (Orphanet:357043) |
Arnold-Chiari malformation type I | (Orphanet:268882) |
Aromatic L-amino acid decarboxylase deficiency | (Orphanet:35708) |
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 | (Orphanet:99947) |
Autosomal dominant dopa-responsive dystonia | (Orphanet:98808) |
Autosomal dominant spastic paraplegia type 10 | (Orphanet:100991) |
Autosomal dominant spastic paraplegia type 12 | (Orphanet:100993) |
Autosomal dominant spastic paraplegia type 13 | (Orphanet:100994) |
Autosomal dominant spastic paraplegia type 17 | (Orphanet:100998) |
Autosomal dominant spastic paraplegia type 19 | (Orphanet:100999) |
Autosomal dominant spastic paraplegia type 29 | (Orphanet:101009) |
Autosomal dominant spastic paraplegia type 3 | (Orphanet:100984) |
Autosomal dominant spastic paraplegia type 31 | (Orphanet:101011) |
Autosomal dominant spastic paraplegia type 36 | (Orphanet:320365) |
Autosomal dominant spastic paraplegia type 37 | (Orphanet:171612) |
Autosomal dominant spastic paraplegia type 38 | (Orphanet:171617) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
Autosomal dominant spastic paraplegia type 42 | (Orphanet:171863) |
Autosomal dominant spastic paraplegia type 6 | (Orphanet:100988) |
Autosomal dominant spastic paraplegia type 8 | (Orphanet:100989) |
Autosomal dominant spastic paraplegia type 9 | (Orphanet:100990) |
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit | (Orphanet:284282) |
Autosomal recessive cerebellar ataxia - saccadic intrusion | (Orphanet:95434) |
Autosomal recessive nonsyndromic intellectual deficit | (Orphanet:88616) |
Autosomal recessive spastic ataxia - optic atrophy - dysarthria | (Orphanet:254343) |
Autosomal recessive spastic ataxia of Charlevoix-Saguenay | (Orphanet:98) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Autosomal recessive spastic paraplegia type 14 | (Orphanet:100995) |
Autosomal recessive spastic paraplegia type 15 | (Orphanet:100996) |
Autosomal recessive spastic paraplegia type 18 | (Orphanet:209951) |
Autosomal recessive spastic paraplegia type 20 | (Orphanet:101000) |
Autosomal recessive spastic paraplegia type 21 | (Orphanet:101001) |
Autosomal recessive spastic paraplegia type 23 | (Orphanet:101003) |
Autosomal recessive spastic paraplegia type 26 | (Orphanet:101006) |
Autosomal recessive spastic paraplegia type 27 | (Orphanet:101007) |
Autosomal recessive spastic paraplegia type 28 | (Orphanet:101008) |
Autosomal recessive spastic paraplegia type 30 | (Orphanet:101010) |
Autosomal recessive spastic paraplegia type 32 | (Orphanet:171622) |
Autosomal recessive spastic paraplegia type 35 | (Orphanet:171629) |
Autosomal recessive spastic paraplegia type 39 | (Orphanet:139480) |
Autosomal recessive spastic paraplegia type 43 | (Orphanet:320370) |
Autosomal recessive spastic paraplegia type 44 | (Orphanet:320401) |
Autosomal recessive spastic paraplegia type 45 | (Orphanet:320396) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
Autosomal recessive spastic paraplegia type 54 | (Orphanet:320380) |
Autosomal recessive spastic paraplegia type 55 | (Orphanet:320375) |
Autosomal recessive spastic paraplegia type 56 | (Orphanet:320411) |
Autosomal recessive spastic paraplegia type 5A | (Orphanet:100986) |
Autosomal recessive spastic paraplegia type 7 | (Orphanet:99013) |
Behavioral variant of frontotemporal dementia | (Orphanet:275864) |
Behr syndrome | (Orphanet:1239) |
Beta-mannosidosis | (Orphanet:118) |
Bilateral frontoparietal polymicrogyria | (Orphanet:101070) |
CAMOS syndrome | (Orphanet:83472) |
CARASIL | (Orphanet:199354) |
CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 1 | (OMIM:603513) |
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED | (OMIM:302900) |
CHOROID PLEXUS CALCIFICATION AND MENTAL RETARDATION | (OMIM:215480) |
Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia | (Orphanet:284324) |
Christianson syndrome | (Orphanet:85278) |
Classical phenylketonuria | (Orphanet:79254) |
Congenital cataracts - facial dysmorphism - neuropathy | (Orphanet:48431) |
Congenital muscular dystrophy type 1A | (Orphanet:258) |
DPM3-CDG | (Orphanet:263494) |
Distal hereditary motor neuropathy type 1 | (Orphanet:139518) |
Distal hereditary motor neuropathy, Jerash type | (Orphanet:139552) |
ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD | (OMIM:130950) |
EPILEPSY, PROGRESSIVE MYOCLONIC, 1B | (OMIM:612437) |
Early-onset X-linked optic atrophy | (Orphanet:98890) |
Early-onset progressive neurodegeneration - blindness - ataxia - spasticity | (Orphanet:352654) |
Encephalopathy due to GLUT1 deficiency | (Orphanet:71277) |
Encephalopathy due to prosaposin deficiency | (Orphanet:139406) |
Episodic ataxia type 1 | (Orphanet:37612) |
FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA | (OMIM:229310) |
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2 | (OMIM:615911) |
Friedreich ataxia 1 | (OMIM:229300) |
Friedreich ataxia 2 | (OMIM:601992) |
Hereditary continuous muscle fiber activity | (Orphanet:972) |
Hereditary motor and sensory neuropathy type 5 | (Orphanet:64751) |
Hereditary sensory and autonomic neuropathy with spastic paraplegia | (Orphanet:139578) |
Hypomyelination - congenital cataract | (Orphanet:85163) |
Hypomyelination with brain stem and spinal cord involvement and leg spasticity | (Orphanet:363412) |
Infantile-onset ascending hereditary spastic paralysis | (Orphanet:293168) |
Inherited congenital spastic tetraplegia | (Orphanet:210141) |
Intellectual deficit, X-linked - psychosis - macroorchidism | (Orphanet:3077) |
Isolated NADH-CoQ reductase deficiency | (Orphanet:2609) |
Isolated succinate-CoQ reductase deficiency | (Orphanet:3208) |
Juvenile amyotrophic lateral sclerosis | (Orphanet:300605) |
Juvenile primary lateral sclerosis | (Orphanet:247604) |
Kufor-Rakeb syndrome | (Orphanet:306674) |
Leber plus disease | (Orphanet:99718) |
Leigh syndrome | (Orphanet:506) |
Lesch-Nyhan syndrome | (Orphanet:510) |
Leukoencephalopathy - ataxia - hypodontia - hypomyelination | (Orphanet:137639) |
Leukoencephalopathy - metaphyseal chondrodysplasia | (Orphanet:83629) |
Leukoencephalopathy with brain stem and spinal cord involvement - lactate elevation | (Orphanet:137898) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 9 | (OMIM:614255) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40 | (OMIM:615599) |
METACHROMATIC LEUKODYSTROPHY | (OMIM:250100) |
METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY | (OMIM:249900) |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 | (OMIM:615157) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 6 | (OMIM:608840) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
Mucolipidosis type 4 | (Orphanet:578) |
Multiple system atrophy | (Orphanet:102) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B | (OMIM:610217) |
NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX | (OMIM:162370) |
NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUALPATHWAY AND AUTONOMIC DISTURBANCE | (OMIM:162380) |
NEUROPATHY, HEREDITARY SENSORY, ATYPICAL | (OMIM:256860) |
Nasu-Hakola disease | (Orphanet:2770) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
Neuroferritinopathy | (Orphanet:157846) |
Odontoleukodystrophy | (Orphanet:77295) |
PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET | (OMIM:260300) |
PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATIONSYNDROME | (OMIM:606721) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 2B | (OMIM:612389) |
PORENCEPHALY 1 | (OMIM:175780) |
Paraplegia - brachydactyly - cone-shaped epiphysis | (Orphanet:2823) |
Parkinsonim due to ATP13A2 deficiency | (Orphanet:314632) |
Pelizaeus-Merzbacher-like due to GJC2 mutation | (Orphanet:280282) |
Pelizaeus-Merzbacher-like due to HSPD1 mutation | (Orphanet:280288) |
Peroxisomal acyl-CoA oxidase deficiency | (Orphanet:2971) |
Polyneuropathy - hearing loss - ataxia - retinitis pigmentosa - cataract | (Orphanet:171848) |
Porencephaly | (Orphanet:2940) |
Primary lateral sclerosis | (Orphanet:35689) |
RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL | (OMIM:614498) |
SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE | (OMIM:611302) |
SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE | (OMIM:614066) |
SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE | (OMIM:612936) |
SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE | (OMIM:613744) |
SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE | (OMIM:614067) |
SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE | (OMIM:615658) |
SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE | (OMIM:615625) |
SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT | (OMIM:616282) |
SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION | (OMIM:607565) |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18 | (OMIM:616204) |
STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL | (OMIM:500003) |
Severe intellectual deficit and progressive spastic paraplegia | (Orphanet:280763) |
Spastic ataxia with congenital miosis | (Orphanet:1182) |
Spastic paraplegia 33, autosomal dominant | (OMIM:610244) |
Spastic paraplegia 64, autosomal recessive | (OMIM:615683) |
Spastic paraplegia type 2 | (Orphanet:99015) |
Spinocerebellar ataxia - dysmorphism | (Orphanet:1185) |
Spinocerebellar ataxia type 1 | (Orphanet:98755) |
Spinocerebellar ataxia type 18 | (Orphanet:98771) |
Spinocerebellar ataxia type 23 | (Orphanet:101108) |
Spinocerebellar ataxia type 25 | (Orphanet:101111) |
Spinocerebellar ataxia type 28 | (Orphanet:101109) |
Spinocerebellar ataxia type 3 | (Orphanet:98757) |
Spinocerebellar ataxia type 35 | (Orphanet:276193) |
Spinocerebellar ataxia type 36 | (Orphanet:276198) |
Spinocerebellar ataxia type 4 | (Orphanet:98765) |
Spinocerebellar ataxia type 7 | (Orphanet:94147) |
Syndromic X-linked intellectual deficit due to JARID1C mutation | (Orphanet:85279) |
Syringomyelia | (Orphanet:3280) |
TRICHORRHEXIS NODOSA SYNDROME | (OMIM:275550) |
Thiamine-responsive encephalopathy | (Orphanet:199348) |
Triple A syndrome | (Orphanet:869) |
X-linked Charcot-Marie-Tooth disease type 1 | (Orphanet:101075) |
X-linked parkinsonism-spasticity syndrome | (Orphanet:363654) |
X-linked sideroblastic anemia - ataxia | (Orphanet:2802) |
X-linked spastic paraplegia type 16 | (Orphanet:100997) |
X-linked spastic paraplegia type 34 | (Orphanet:171607) |
[DEL] SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE | (OMIM:607259) |