Reduced tendon reflexes
Symptom Information:
Symptom ID: | HPO:0001315 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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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) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Abnormal reflexes(MedDRA:10000171) Reduced tendon reflexes(HPO:0001315) |
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Database Frequency: | 160 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
3-methylglutaconic aciduria type 4 | (Orphanet:67048) |
ATAXIA-TELANGIECTASIA | (OMIM:208900) |
Abetalipoproteinemia | (Orphanet:14) |
Adducted thumbs - arthrogryposis, Christian type | (Orphanet:2952) |
Adult polyglucosan body disease | (Orphanet:206583) |
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency | (Orphanet:329314) |
Arachnoiditis | (Orphanet:137817) |
Arthrogryposis due to muscular dystrophy | (Orphanet:1155) |
Arthrogryposis-like syndrome | (Orphanet:1149) |
Ataxia - photosensitivity - short stature | (Orphanet:1184) |
Ataxia with vitamin E deficiency | (Orphanet:96) |
Ataxia-deafness-retardation syndrome | (Orphanet:1188) |
Ataxia-telangiectasia | (Orphanet:100) |
Autosomal dominant Emery-Dreifuss muscular dystrophy | (Orphanet:98853) |
Autosomal dominant cerebellar ataxia | (Orphanet:99) |
Autosomal dominant limb-girdle muscular dystrophy type 1A | (Orphanet:266) |
Autosomal dominant optic atrophy plus syndrome | (Orphanet:1215) |
Autosomal recessive Emery-Dreifuss muscular dystrophy | (Orphanet:98855) |
Autosomal recessive cerebelloparenchymal disorder type 3 | (Orphanet:1170) |
Autosomal recessive limb-girdle muscular dystrophy type 2M | (Orphanet:206554) |
Autosomal recessive spastic ataxia - optic atrophy - dysarthria | (Orphanet:254343) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Autosomal recessive spastic paraplegia type 26 | (Orphanet:101006) |
Autosomal recessive spastic paraplegia type 43 | (Orphanet:320370) |
Becker muscular dystrophy | (Orphanet:98895) |
CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS | (OMIM:606842) |
CEDNIK syndrome | (Orphanet:66631) |
CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM | (OMIM:118301) |
CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE | (OMIM:118230) |
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED | (OMIM:302900) |
COFS syndrome | (Orphanet:1466) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Carnitine palmitoyl transferase 1A deficiency | (Orphanet:156) |
Cartilage-hair hypoplasia | (Orphanet:175) |
Cataract - ataxia - deafness | (Orphanet:1368) |
Caudal regression sequence | (Orphanet:3027) |
Centronuclear myopathy | (Orphanet:595) |
Cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss | (Orphanet:1171) |
Charcot-Marie-Tooth disease | (Orphanet:166) |
Choreoacanthocytosis | (Orphanet:2388) |
Chylomicron retention disease | (Orphanet:71) |
Chédiak-Higashi syndrome | (Orphanet:167) |
Cogan syndrome | (Orphanet:1467) |
Combined oxidative phosphorylation defect type 8 | (Orphanet:319504) |
Congenital fiber-type disproportion myopathy | (Orphanet:2020) |
Congenital hypothyroidism | (Orphanet:442) |
Congenital muscular dystrophy type 1A | (Orphanet:258) |
Cortical dysplasia - focal epilepsy syndrome | (Orphanet:163681) |
DE SANCTIS-CACCHIONE SYNDROME | (OMIM:278800) |
DPM3-CDG | (Orphanet:263494) |
Deafness - small bowel diverticulosis - neuropathy | (Orphanet:3217) |
Deafness - enamel hypoplasia - nail defects | (Orphanet:3220) |
Dermatoleukodystrophy | (Orphanet:1659) |
Early-onset X-linked optic atrophy | (Orphanet:98890) |
Emery-Dreifuss muscular dystrophy | (Orphanet:261) |
Erythrokeratodermia - ataxia | (Orphanet:1955) |
FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA | (OMIM:229310) |
Familial dysautonomia | (Orphanet:1764) |
Familial symmetric lipomatosis | (Orphanet:2398) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
Friedreich ataxia 1 | (OMIM:229300) |
Friedreich ataxia 2 | (OMIM:601992) |
Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
Glycogen storage disease due to glycogen branching enzyme deficiency | (Orphanet:367) |
Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form | (Orphanet:308712) |
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form | (Orphanet:308684) |
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form | (Orphanet:308698) |
Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form | (Orphanet:308670) |
Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form | (Orphanet:308655) |
Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form | (Orphanet:308638) |
Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form | (Orphanet:308621) |
Griscelli disease | (Orphanet:381) |
Grubben-de Cock-Borghgraef syndrome | (Orphanet:2101) |
HYPOBETALIPOPROTEINEMIA, FAMILIAL, 1 | (OMIM:615558) |
Hemihypertrophy | (Orphanet:2128) |
Hennekam-Beemer syndrome | (Orphanet:2135) |
Hereditary neuropathy with liability to pressure palsies | (Orphanet:640) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Hyperkalemic periodic paralysis | (Orphanet:682) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Hypomyelination neuropathy - arthrogryposis | (Orphanet:2680) |
Ichthyosis - hepatosplenomegaly - cerebellar degeneration | (Orphanet:2274) |
Inclusion body myositis | (Orphanet:611) |
Infant botulism | (Orphanet:178478) |
Infantile axonal neuropathy | (Orphanet:2679) |
Infantile onset spinocerebellar ataxia | (Orphanet:1186) |
Intellectual deficit, X-linked, Stevenson type | (Orphanet:85325) |
Isolated glycerol kinase deficiency | (Orphanet:408) |
Isotretinoin syndrome | (Orphanet:2305) |
KID syndrome | (Orphanet:477) |
Kearns-Sayre syndrome | (Orphanet:480) |
Kennedy disease | (Orphanet:481) |
Leigh syndrome | (Orphanet:506) |
Lethal ataxia with deafness and optic atrophy | (Orphanet:1187) |
Linear nevus sebaceus syndrome | (Orphanet:2612) |
MELAS | (Orphanet:550) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 13 | (OMIM:614563) |
METACHROMATIC LEUKODYSTROPHY | (OMIM:250100) |
MITOCHONDRIAL MYOPATHY | (OMIM:251900) |
MYOGLOBINURIA, ACUTE RECURRENT, AUTOSOMAL RECESSIVE | (OMIM:268200) |
MYOPATHY, REDUCING BODY, X-LINKED, EARLY-ONSET, SEVERE | (OMIM:300717) |
Maple syrup urine disease | (Orphanet:511) |
Marden-Walker syndrome | (Orphanet:2461) |
Marinesco-Sjögren syndrome | (Orphanet:559) |
Maternally-inherited Leigh syndrome | (Orphanet:255210) |
Metachromatic leukodystrophy | (Orphanet:512) |
Microlissencephaly - micromelia | (Orphanet:50810) |
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria | (Orphanet:1933) |
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency | (Orphanet:254864) |
Mulibrey nanism | (Orphanet:2576) |
Multifocal muscular fibrosis - obstructed vessels | (Orphanet:2033) |
Muscular dystrophy - white matter spongiosis | (Orphanet:1877) |
Myopathy and diabetes mellitus | (Orphanet:2596) |
Myopathy due to myoadenylate deaminase deficiency | (OMIM:615511) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A | (OMIM:256600) |
Neuhauser-Eichner-Opitz syndrome | (Orphanet:2672) |
Neuralgic amyotrophy | (Orphanet:2901) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
Neutral lipid storage disease | (Orphanet:165) |
Neutral lipid storage myopathy | (Orphanet:98908) |
Niemann-Pick disease type A | (Orphanet:77292) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Orofaciodigital syndrome type 3 | (Orphanet:2752) |
POSTERIOR COLUMN ATAXIA | (OMIM:176250) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 5 | (OMIM:613077) |
Pellagra-like skin rash-neurological manifestations | (Orphanet:2837) |
Peripheral motor neuropathy - dysautonomia | (Orphanet:2400) |
Perrault Syndrome 1 | (OMIM:233400) |
Polymyositis | (Orphanet:732) |
Polyneuropathy - intellectual deficit - acromicria - premature menopause | (Orphanet:2928) |
Protein R deficiency | (Orphanet:2967) |
Proximal spinal muscular atrophy | (Orphanet:70) |
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | (Orphanet:88618) |
Qazi-Markouizos syndrome | (Orphanet:3010) |
Riboflavin transporter deficiency | (Orphanet:97229) |
Roussy-Lévy syndrome | (Orphanet:3115) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Short stature - heart defect - craniofacial anomalies | (Orphanet:1088) |
Smith-Magenis syndrome | (Orphanet:819) |
Spastic paraplegia 64, autosomal recessive | (OMIM:615683) |
Spinocerebellar ataxia - dysmorphism | (Orphanet:1185) |
Stoll-Alembik-Finck syndrome | (Orphanet:3200) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |
Sudden infant death - dysgenesis of the testes | (Orphanet:168593) |
Symmetrical thalamic calcifications | (Orphanet:1314) |
TMCO1 defect syndrome | (Orphanet:228407) |
Tangier disease | (Orphanet:31150) |
Tetrasomy 12p | (Orphanet:884) |
Thoracic dysplasia-hydrocephalus syndrome | (Orphanet:1861) |
Tyrosinemia type 3 | (Orphanet:69723) |
Walker-Warburg syndrome | (Orphanet:899) |
X-linked Charcot-Marie-Tooth disease type 1 | (Orphanet:101075) |
X-linked Charcot-Marie-Tooth disease type 2 | (Orphanet:101076) |
X-linked Charcot-Marie-Tooth disease type 4 | (Orphanet:101078) |
X-linked Charcot-Marie-Tooth disease type 5 | (Orphanet:99014) |
X-linked Emery-Dreifuss muscular dystrophy | (Orphanet:98863) |
X-linked centronuclear myopathy | (Orphanet:596) |
Xeroderma pigmentosum | (Orphanet:910) |
Zellweger syndrome | (Orphanet:912) |
Zellweger-like syndrome without peroxisomal anomalies | (Orphanet:50812) |