Areflexia
Symptom Information:
Symptom ID: | HPO:0001284 | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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) Reduced tendon reflexes(HPO:0001315) Areflexia(HPO:0001284) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Abnormal reflexes(MedDRA:10000171) Areflexia(HPO:0001284) |
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Database Frequency: | 198 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
3-methylglutaconic aciduria type 4 | (Orphanet:67048) |
ALG1-CDG | (Orphanet:79327) |
ALG6-CDG | (Orphanet:79320) |
AMYOTROPHIC LATERAL SCLEROSIS 17 | (OMIM:614696) |
AMYOTROPHIC LATERAL SCLEROSIS 8 | (OMIM:608627) |
ATAXIA, SENSORY, 1, AUTOSOMAL DOMINANT | (OMIM:608984) |
ATAXIA-OCULOMOTOR APRAXIA 3 | (OMIM:615217) |
ATAXIA-OCULOMOTOR APRAXIA 4 | (OMIM:616267) |
ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3 | (OMIM:170995) |
Alagille syndrome due to 20p12 microdeletion | (Orphanet:261600) |
Alagille syndrome due to a JAG1 point mutation | (Orphanet:261619) |
Alpha-mannosidosis | (Orphanet:61) |
Ataxia - hypogonadism - choroidal dystrophy | (Orphanet:1180) |
Ataxia - oculomotor apraxia type 1 | (Orphanet:1168) |
Ataxia with vitamin E deficiency | (Orphanet:96) |
Autosomal dominant Charcot-Marie-Tooth disease type 2A1 | (Orphanet:99946) |
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 | (Orphanet:99947) |
Autosomal dominant Charcot-Marie-Tooth disease type 2B | (Orphanet:99936) |
Autosomal dominant Charcot-Marie-Tooth disease type 2C | (Orphanet:99937) |
Autosomal dominant Charcot-Marie-Tooth disease type 2E | (Orphanet:99939) |
Autosomal dominant Charcot-Marie-Tooth disease type 2F | (Orphanet:99940) |
Autosomal dominant Charcot-Marie-Tooth disease type 2G | (Orphanet:99941) |
Autosomal dominant Charcot-Marie-Tooth disease type 2I | (Orphanet:99942) |
Autosomal dominant Charcot-Marie-Tooth disease type 2J | (Orphanet:99943) |
Autosomal dominant Charcot-Marie-Tooth disease type 2K | (Orphanet:99944) |
Autosomal dominant Charcot-Marie-Tooth disease type 2L | (Orphanet:99945) |
Autosomal dominant Charcot-Marie-Tooth disease type 2M | (Orphanet:228179) |
Autosomal dominant Charcot-Marie-Tooth disease type 2N | (Orphanet:228174) |
Autosomal dominant Charcot-Marie-Tooth disease type 2P | (Orphanet:300319) |
Autosomal dominant centronuclear myopathy | (Orphanet:169189) |
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures | (Orphanet:363454) |
Autosomal dominant congenital benign spinal muscular atrophy | (Orphanet:1216) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type A | (Orphanet:100043) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B | (Orphanet:100044) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type D | (Orphanet:100046) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E | (Orphanet:93114) |
Autosomal dominant limb-girdle muscular dystrophy type 1A | (Orphanet:266) |
Autosomal recessive Charcot-Marie-Tooth disease with hoarseness | (Orphanet:101097) |
Autosomal recessive centronuclear myopathy | (Orphanet:169186) |
Autosomal recessive cerebelloparenchymal disorder type 3 | (Orphanet:1170) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A | (Orphanet:217055) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type B | (Orphanet:254334) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type C | (Orphanet:369867) |
Autosomal recessive limb-girdle muscular dystrophy type 2H | (Orphanet:1878) |
Autosomal recessive limb-girdle muscular dystrophy type 2M | (Orphanet:206554) |
Autosomal recessive lower motor neuron disease with childhood onset | (Orphanet:206580) |
Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
Autosomal recessive spastic ataxia - optic atrophy - dysarthria | (Orphanet:254343) |
Autosomal recessive spastic paraplegia type 26 | (Orphanet:101006) |
Autosomal recessive spastic paraplegia type 43 | (Orphanet:320370) |
Autosomal recessive spastic paraplegia type 49 | (Orphanet:320385) |
BROWN-VIALETTO-VAN LAERE SYNDROME 2 | (OMIM:614707) |
CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS | (OMIM:606842) |
CEDNIK syndrome | (Orphanet:66631) |
CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURALHEARING LOSS | (OMIM:601338) |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R | (OMIM:615490) |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S | (OMIM:616155) |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U | (OMIM:616280) |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE | (OMIM:607706) |
CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D | (OMIM:616039) |
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED | (OMIM:302900) |
Cataract - ataxia - deafness | (Orphanet:1368) |
Charcot-Marie-Tooth disease type 1A | (Orphanet:101081) |
Charcot-Marie-Tooth disease type 1B | (Orphanet:101082) |
Charcot-Marie-Tooth disease type 1E | (Orphanet:90658) |
Charcot-Marie-Tooth disease type 1F | (Orphanet:101085) |
Charcot-Marie-Tooth disease type 2B1 | (Orphanet:98856) |
Charcot-Marie-Tooth disease type 2B2 | (Orphanet:101101) |
Charcot-Marie-Tooth disease type 4A | (Orphanet:99948) |
Charcot-Marie-Tooth disease type 4B2 | (Orphanet:99956) |
Charcot-Marie-Tooth disease type 4B3 | (Orphanet:363981) |
Charcot-Marie-Tooth disease type 4D | (Orphanet:99950) |
Charcot-Marie-Tooth disease type 4E | (Orphanet:99951) |
Charcot-Marie-Tooth disease type 4F | (Orphanet:99952) |
Charcot-Marie-Tooth disease type 4H | (Orphanet:99954) |
Charcot-Marie-Tooth disease type 4J | (Orphanet:139515) |
Choreoacanthocytosis | (Orphanet:2388) |
Chronic intestinal pseudo-obstruction | (Orphanet:2978) |
Combined oxidative phosphorylation defect type 11 | (Orphanet:324535) |
Combined oxidative phosphorylation defect type 7 | (Orphanet:254930) |
Congenital lethal myopathy, Compton-North type | (Orphanet:210163) |
Congenital multicore myopathy with external ophthalmoplegia | (Orphanet:98905) |
Congenital muscular dystrophy type 1A | (Orphanet:258) |
Congenital myopathy with excess of thin filaments | (Orphanet:98904) |
Corpus callosum agenesis - neuronopathy | (Orphanet:1496) |
DE SANCTIS-CACCHIONE SYNDROME | (OMIM:278800) |
Deafness - encephaloneuropathy - obesity - valvulopathy | (Orphanet:254898) |
Dejerine-Sottas syndrome | (Orphanet:64748) |
ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD | (OMIM:130950) |
EPILEPSY, PROGRESSIVE MYOCLONIC, 5 | (OMIM:613832) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29 | (OMIM:616339) |
Early-onset X-linked optic atrophy | (Orphanet:98890) |
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2 | (OMIM:615911) |
Fetal akinesia-cerebral and retinal hemorrhage syndrome | (Orphanet:363409) |
Friedreich ataxia 2 | (OMIM:601992) |
GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT | (OMIM:610100) |
Genetic recurrent myoglobinuria | (Orphanet:99845) |
Gerstmann-Straussler-Scheinker syndrome | (Orphanet:356) |
Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
Glycogen storage disease due to glycogen branching enzyme deficiency | (Orphanet:367) |
Hereditary motor and sensory neuropathy type 6 | (Orphanet:90120) |
Hereditary myoclonus - progressive distal muscular atrophy | (Orphanet:2590) |
Hereditary sensory and autonomic neuropathy type 1 | (Orphanet:36386) |
Hereditary sensory and autonomic neuropathy type 2 | (Orphanet:970) |
Hereditary sensory and autonomic neuropathy type 6 | (Orphanet:314381) |
Hereditary thermosensitive neuropathy | (Orphanet:84093) |
Infantile cerebellar-retinal degeneration | (Orphanet:313850) |
Infantile neuroaxonal dystrophy | (Orphanet:35069) |
Infantile onset spinocerebellar ataxia | (Orphanet:1186) |
Intellectual disability-developmental delay-contractures syndrome | (Orphanet:3454) |
Kearns-Sayre syndrome | (Orphanet:480) |
LETHAL CONGENITAL CONTRACTURE SYNDROME 7 | (OMIM:616286) |
LETHAL CONGENITAL CONTRACTURE SYNDROME 8 | (OMIM:616287) |
LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA | (OMIM:616342) |
Lethal ataxia with deafness and optic atrophy | (Orphanet:1187) |
Lethal encephalopathy due to mitochondrial and peroxisomal fission defect | (Orphanet:330050) |
Lower motor neuron syndrome with late-adult onset | (Orphanet:276435) |
MELAS | (Orphanet:550) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 13 | (OMIM:614563) |
METACHROMATIC LEUKODYSTROPHY | (OMIM:250100) |
MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) | (OMIM:603041) |
MITOCHONDRIAL MYOPATHY | (OMIM:251900) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 4 | (OMIM:253800) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6 | (OMIM:613154) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 7 | (OMIM:614643) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 2 | (OMIM:613156) |
MYASTHENIC SYNDROME, CONGENITAL, 18 | (OMIM:616330) |
MYASTHENIC SYNDROME, CONGENITAL, 7, PRESYNAPTIC | (OMIM:616040) |
MYOGLOBINURIA, ACUTE RECURRENT, AUTOSOMAL RECESSIVE | (OMIM:268200) |
MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET | (OMIM:614399) |
MYOPATHY, CENTRONUCLEAR, 1 | (OMIM:160150) |
MYOPATHY, CENTRONUCLEAR, 5 | (OMIM:615959) |
MYOPATHY, REDUCING BODY, X-LINKED, EARLY-ONSET, SEVERE | (OMIM:300717) |
Maple syrup urine disease | (Orphanet:511) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency | (Orphanet:254864) |
Mitochondrial neurogastrointestinal encephalomyopathy | (Orphanet:298) |
Mitochondrial trifunctional protein deficiency | (Orphanet:746) |
Myopathy and diabetes mellitus | (Orphanet:2596) |
Myotilin-related myofibrillar myopathy without spheroid body | (Orphanet:98911) |
NEMALINE MYOPATHY 2 | (OMIM:256030) |
NEMALINE MYOPATHY 7 | (OMIM:610687) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A | (OMIM:256600) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB | (OMIM:614751) |
NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUALPATHWAY AND AUTONOMIC DISTURBANCE | (OMIM:162380) |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA | (OMIM:201300) |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB | (OMIM:613115) |
NEUROPATHY, HEREDITARY SENSORY, TYPE IIC | (OMIM:614213) |
Navajo neurohepatopathy | (Orphanet:255229) |
Nemaline myopathy | (Orphanet:607) |
Neuralgic amyotrophy | (Orphanet:2901) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |
Neutral lipid storage myopathy | (Orphanet:98908) |
Niemann-Pick disease type A | (Orphanet:77292) |
OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE | (OMIM:258650) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Oculopharyngodistal myopathy | (Orphanet:98897) |
PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS | (OMIM:614369) |
PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER) | (OMIM:214110) |
PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER) | (OMIM:614866) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 | (OMIM:609286) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 5 | (OMIM:613077) |
Perrault Syndrome | (Orphanet:2855) |
Perrault Syndrome 1 | (OMIM:233400) |
Pierson syndrome | (Orphanet:2670) |
Posterior column ataxia - retinitis pigmentosa | (Orphanet:88628) |
Primary CD59 deficiency | (Orphanet:169464) |
Progressive myoclonic epilepsy type 6 | (Orphanet:280620) |
Proximal spinal muscular atrophy | (Orphanet:70) |
Proximal spinal muscular atrophy type 1 | (Orphanet:83330) |
Pyruvate dehydrogenase E1-alpha deficiency | (Orphanet:79243) |
RADICULONEUROPATHY, FATAL NEONATAL | (OMIM:266250) |
Reducing body myopathy | (Orphanet:97239) |
Richards-Rundle syndrome | (Orphanet:1399) |
Roussy-Lévy syndrome | (Orphanet:3115) |
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY | (OMIM:181405) |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 | (OMIM:606002) |
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis | (Orphanet:70595) |
Severe X-linked mitochondrial encephalomyopathy | (Orphanet:238329) |
Smith-Magenis syndrome | (Orphanet:819) |
Spinocerebellar ataxia type 1 | (Orphanet:98755) |
Spinocerebellar ataxia type 18 | (Orphanet:98771) |
Spinocerebellar ataxia type 4 | (Orphanet:98765) |
Spinocerebellar ataxia with axonal neuropathy type 2 | (Orphanet:64753) |
Spinocerebellar ataxia with epilepsy | (Orphanet:254881) |
TMCO1 defect syndrome | (Orphanet:228407) |
TRICHORRHEXIS NODOSA SYNDROME | (OMIM:275550) |
Tangier disease | (Orphanet:31150) |
VISCERAL NEUROPATHY, FAMILIAL, AUTOSOMAL RECESSIVE | (OMIM:243180) |
Wolfram syndrome 1 | (OMIM:222300) |
X-linked Charcot-Marie-Tooth disease type 2 | (Orphanet:101076) |
X-linked Charcot-Marie-Tooth disease type 3 | (Orphanet:101077) |
X-linked centronuclear myopathy | (Orphanet:596) |
X-linked distal arthrogryposis multiplex congenita | (Orphanet:1145) |
X-linked spinocerebellar ataxia type 3 | (Orphanet:85297) |
Young adult-onset distal hereditary motor neuropathy | (Orphanet:314485) |
Zellweger syndrome | (Orphanet:912) |