Hyperactive deep tendon reflexes
Symptom Information:
Symptom ID: | HPO:0006801 | |||
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) Abnormality of central motor function(HPO:0011442) Abnormal pyramidal signs(HPO:0007256) Hyperreflexia(HPO:0001347) Hyperactive deep tendon reflexes(HPO:0006801) MedDRA: |
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Database Frequency: | 21 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Ataxia - pancytopenia | (Orphanet:2585) |
Autosomal recessive nonsyndromic intellectual deficit | (Orphanet:88616) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Autosomal recessive spastic paraplegia type 45 | (Orphanet:320396) |
CHOROID PLEXUS CALCIFICATION AND MENTAL RETARDATION | (OMIM:215480) |
CHROMOSOME 17p13.1 DELETION SYNDROME | (OMIM:613776) |
Dyschromatosis symmetrica hereditaria | (Orphanet:41) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hyperlysinemia, type I | (OMIM:238700) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Krabbe disease | (Orphanet:487) |
Leigh syndrome | (Orphanet:506) |
Microcephaly-capillary malformation syndrome | (Orphanet:294016) |
OCULODENTODIGITAL DYSPLASIA | (OMIM:164200) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Pontocerebellar hypoplasia, type 9 | (OMIM:615809) |
Pyruvate dehydrogenase E2 deficiency | (Orphanet:79244) |
Simpson-Golabi-Behmel syndrome type 2 | (Orphanet:79022) |
Spastic paraplegia 63, autosomal recessive | (OMIM:615686) |
Spastic paraplegia 64, autosomal recessive | (OMIM:615683) |
X-linked Charcot-Marie-Tooth disease type 5 | (Orphanet:99014) |