Hyporeflexia
Symptom Information:
Symptom ID: | HPO:0001265 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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) Hyporeflexia(HPO:0001265) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Abnormal reflexes(MedDRA:10000171) Hyporeflexia(HPO:0001265) |
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Database Frequency: | 208 / 7739 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
2q37 microdeletion syndrome | (Orphanet:1001) |
3-methylglutaconic aciduria type 4 | (Orphanet:67048) |
4-hydroxybutyric aciduria | (Orphanet:22) |
ADIE PUPIL | (OMIM:103100) |
AMYOTROPHIC LATERAL SCLEROSIS 17 | (OMIM:614696) |
AMYOTROPHIC LATERAL SCLEROSIS 6, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA | (OMIM:608030) |
ATAXIA, SENSORY, 1, AUTOSOMAL DOMINANT | (OMIM:608984) |
ATAXIA-OCULOMOTOR APRAXIA 3 | (OMIM:615217) |
ATTRV122I amyloidosis | (Orphanet:85451) |
Adult-onset proximal spinal muscular atrophy, autosomal dominant | (Orphanet:209335) |
Ataxia - hypogonadism - choroidal dystrophy | (Orphanet:1180) |
Ataxia - oculomotor apraxia type 1 | (Orphanet:1168) |
Ataxia-telangiectasia-like disorder | (Orphanet:251347) |
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 2D | (Orphanet:99938) |
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 2L | (Orphanet:99945) |
Autosomal dominant Charcot-Marie-Tooth disease type 2M | (Orphanet:228179) |
Autosomal dominant Charcot-Marie-Tooth disease type 2O | (Orphanet:284232) |
Autosomal dominant Charcot-Marie-Tooth disease type 2P | (Orphanet:300319) |
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 intermediate Charcot-Marie-Tooth disease type F | (Orphanet:352670) |
Autosomal dominant limb-girdle muscular dystrophy type 1A | (Orphanet:266) |
Autosomal dominant limb-girdle muscular dystrophy type 1H | (Orphanet:238755) |
Autosomal dominant progressive external ophthalmoplegia | (Orphanet:254892) |
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit | (Orphanet:284282) |
Autosomal recessive cerebelloparenchymal disorder type 3 | (Orphanet:1170) |
Autosomal recessive deafness-onychodystrophy syndrome | (Orphanet:79500) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A | (Orphanet:217055) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type B | (Orphanet:254334) |
Autosomal recessive limb-girdle muscular dystrophy type 2H | (Orphanet:1878) |
Autosomal recessive limb-girdle muscular dystrophy type 2M | (Orphanet:206554) |
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) |
BARTTER SYNDROME, TYPE 4A | (OMIM:602522) |
BARTTER SYNDROME, TYPE 4B | (OMIM:613090) |
CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS | (OMIM:606842) |
CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURALHEARING LOSS, AND SKELETAL DYSPLASIA | (OMIM:616007) |
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2 | (OMIM:610185) |
CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME | (OMIM:614575) |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S | (OMIM:616155) |
CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D | (OMIM:616039) |
Channelopathy-associated congenital insensitivity to pain | (Orphanet:88642) |
Charcot-Marie-Tooth disease type 1A | (Orphanet:101081) |
Charcot-Marie-Tooth disease type 1B | (Orphanet:101082) |
Charcot-Marie-Tooth disease type 1C | (Orphanet:101083) |
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 4D | (Orphanet:99950) |
Charcot-Marie-Tooth disease type 4G | (Orphanet:99953) |
Charcot-Marie-Tooth disease type 4H | (Orphanet:99954) |
Charcot-Marie-Tooth disease type 4J | (Orphanet:139515) |
Choreoacanthocytosis | (Orphanet:2388) |
Chédiak-Higashi syndrome | (Orphanet:167) |
Combined oxidative phosphorylation defect type 11 | (Orphanet:324535) |
Combined oxidative phosphorylation defect type 13 | (Orphanet:319514) |
Congenital muscular dystrophy type 1A | (Orphanet:258) |
Congenital myopathy with excess of thin filaments | (Orphanet:98904) |
DE SANCTIS-CACCHIONE SYNDROME | (OMIM:278800) |
Dejerine-Sottas syndrome | (Orphanet:64748) |
Distal hereditary motor neuropathy type 7 | (Orphanet:139589) |
Distal hereditary motor neuropathy, Jerash type | (Orphanet:139552) |
Distal myopathy with posterior leg and anterior hand involvement | (Orphanet:63273) |
Dopa-responsive dystonia due to sepiapterin reductase deficiency | (Orphanet:70594) |
Duchenne muscular dystrophy | (Orphanet:98896) |
Early infantile epileptic encephalopathy without suppression burst | (Orphanet:369894) |
Early-onset X-linked optic atrophy | (Orphanet:98890) |
Erythrokeratodermia - ataxia | (Orphanet:1955) |
FACIAL SPASM | (OMIM:134300) |
FRIEDREICH ATAXIA, SO-CALLED, WITH OPTIC ATROPHY AND SENSORINEURALDEAFNESS | (OMIM:136600) |
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2 | (OMIM:615911) |
Familial amyloid polyneuropathy | (Orphanet:85447) |
Familial dysautonomia | (Orphanet:1764) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
Friedreich ataxia 2 | (OMIM:601992) |
GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT | (OMIM:610100) |
Gaucher disease - ophthalmoplegia - cardiovascular calcification | (Orphanet:2072) |
Genetic recurrent myoglobinuria | (Orphanet:99845) |
Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
Hereditary motor and sensory neuropathy type 6 | (Orphanet:90120) |
Hereditary neuropathy with liability to pressure palsies | (Orphanet:640) |
Hereditary sensory and autonomic neuropathy type 1 | (Orphanet:36386) |
Hereditary sensory and autonomic neuropathy type 2 | (Orphanet:970) |
Inclusion body myositis | (Orphanet:611) |
Infantile Bartter syndrome with deafness | (Orphanet:89938) |
Infantile cerebellar-retinal degeneration | (Orphanet:313850) |
Infantile onset spinocerebellar ataxia | (Orphanet:1186) |
Isolated NADH-CoQ reductase deficiency | (Orphanet:2609) |
KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY | (OMIM:611722) |
Kearns-Sayre syndrome | (Orphanet:480) |
Kennedy disease | (Orphanet:481) |
Leigh syndrome | (Orphanet:506) |
Leukoencephalopathy with brain stem and spinal cord involvement - lactate elevation | (Orphanet:137898) |
Lower motor neuron syndrome with late-adult onset | (Orphanet:276435) |
MELAS | (Orphanet:550) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 13 | (OMIM:614563) |
METACHROMATIC LEUKODYSTROPHY | (OMIM:250100) |
METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY | (OMIM:249900) |
MITOCHONDRIAL MYOPATHY | (OMIM:251900) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 2 | (OMIM:613156) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12 | (OMIM:616094) |
MYASTHENIC SYNDROME, CONGENITAL, 17 | (OMIM:616304) |
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, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET | (OMIM:300718) |
MYOPATHY, REDUCING BODY, X-LINKED, EARLY-ONSET, SEVERE | (OMIM:300717) |
Maple syrup urine disease | (Orphanet:511) |
Maternally-inherited Leigh syndrome | (Orphanet:255210) |
Microcephaly - seizures - developmental delay | (Orphanet:228418) |
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria | (Orphanet:1933) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency | (Orphanet:254864) |
Monosomy 22q13 | (Orphanet:48652) |
Multiple congenital anomalies - hypotonia - seizures syndrome | (Orphanet:280633) |
Muscular dystrophy, Selcen type | (Orphanet:199340) |
Myopathy and diabetes mellitus | (Orphanet:2596) |
NEMALINE MYOPATHY 2 | (OMIM:256030) |
NEMALINE MYOPATHY 4 | (OMIM:609285) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A | (OMIM:256600) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6 | (OMIM:615643) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB | (OMIM:614751) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA | (OMIM:158580) |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA | (OMIM:201300) |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB | (OMIM:613115) |
NEUROPATHY, HEREDITARY SENSORY, TYPE IE | (OMIM:614116) |
NEUROPATHY, HEREDITARY SENSORY, TYPE IIC | (OMIM:614213) |
Native American myopathy | (Orphanet:168572) |
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) |
PELIZAEUS-MERZBACHER DISEASE | (OMIM:312080) |
PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS | (OMIM:614369) |
PEROXISOME BIOGENESIS DISORDER 3B | (OMIM:266510) |
PEROXISOME BIOGENESIS DISORDER 5B | (OMIM:614867) |
PEROXISOME BIOGENESIS DISORDER 6B | (OMIM:614871) |
PMM2-CDG | (Orphanet:79318) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 | (OMIM:157640) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 | (OMIM:609286) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 5 | (OMIM:613077) |
PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM | (OMIM:614501) |
Perrault Syndrome | (Orphanet:2855) |
Perrault Syndrome 1 | (OMIM:233400) |
Perrault Syndrome 5 | (OMIM:616138) |
Polymicrogyria with optic nerve hypoplasia | (Orphanet:250972) |
Polyneuropathy - hearing loss - ataxia - retinitis pigmentosa - cataract | (Orphanet:171848) |
Progressive demyelinating neuropathy with bilateral striatal necrosis | (Orphanet:217396) |
Progressive external ophthalmoplegia - myopathy - emaciation | (Orphanet:352447) |
Proximal spinal muscular atrophy type 3 | (Orphanet:83419) |
Pyruvate dehydrogenase E1-alpha deficiency | (Orphanet:79243) |
Pyruvate dehydrogenase E1-beta deficiency | (Orphanet:255138) |
REFSUM DISEASE, CLASSIC | (OMIM:266500) |
RIENHOFF SYNDROME | (OMIM:615582) |
Reducing body myopathy | (Orphanet:97239) |
Refsum disease | (Orphanet:773) |
Roussy-Lévy syndrome | (Orphanet:3115) |
SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT | (OMIM:300695) |
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY | (OMIM:181405) |
SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1 | (OMIM:604320) |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 15 | (OMIM:615705) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis | (Orphanet:70595) |
Severe X-linked mitochondrial encephalomyopathy | (Orphanet:238329) |
Smith-Magenis syndrome | (Orphanet:819) |
Spastic paraplegia-optic atrophy-neuropathy syndrome | (Orphanet:320406) |
Spinal muscular atrophy with respiratory distress | (Orphanet:98920) |
Spinocerebellar ataxia - dysmorphism | (Orphanet:1185) |
Spinocerebellar ataxia type 18 | (Orphanet:98771) |
Spinocerebellar ataxia type 19/22 | (Orphanet:98772) |
Spinocerebellar ataxia type 2 | (Orphanet:98756) |
Spinocerebellar ataxia type 21 | (Orphanet:98773) |
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) |
Tangier disease | (Orphanet:31150) |
Triose phosphate-isomerase deficiency | (Orphanet:868) |
X-linked Charcot-Marie-Tooth disease type 1 | (Orphanet:101075) |
X-linked distal spinal muscular atrophy | (Orphanet:139557) |
X-linked intellectual disability due to GRIA3 anomalies | (Orphanet:364028) |
X-linked spinocerebellar ataxia type 3 | (Orphanet:85297) |
Xeroderma pigmentosum complementation group A | (Orphanet:276249) |
Xeroderma pigmentosum complementation group D | (Orphanet:276258) |
Xeroderma pigmentosum/Cockayne syndrome complex | (Orphanet:220295) |
Zellweger syndrome | (Orphanet:912) |
[DEL] MUSCULAR DYSTROPHY, BECKER TYPE | (OMIM:300376) |