Abnormality of central motor function
Symptom Information:
| Symptom ID: | HPO:0011442 | ||
| 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) MedDRA: |
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| Database Frequency: | 76 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| 3C syndrome | (Orphanet:7) |
| Adult neuronal ceroid lipofuscinosis | (Orphanet:79262) |
| Adult polyglucosan body disease | (Orphanet:206583) |
| Adult-onset autosomal dominant leukodystrophy | (Orphanet:99027) |
| Alexander disease | (Orphanet:58) |
| Arachnoiditis | (Orphanet:137817) |
| Autosomal recessive cutis laxa type 1 | (Orphanet:90349) |
| Autosomal recessive cutis laxa type 2 | (Orphanet:90350) |
| Autosomal recessive omodysplasia | (Orphanet:93329) |
| Bannayan-Riley-Ruvalcaba syndrome | (Orphanet:109) |
| Benign familial infantile seizures | (Orphanet:306) |
| Canavan disease | (Orphanet:141) |
| Caudal regression sequence | (Orphanet:3027) |
| Chronic mucocutaneous candidiasis | (Orphanet:1334) |
| Classic galactosemia | (Orphanet:79239) |
| Cleidocranial dysplasia | (Orphanet:1452) |
| Cobb syndrome | (Orphanet:53721) |
| Cohen syndrome | (Orphanet:193) |
| Congenital muscular dystrophy due to LMNA mutation | (Orphanet:157973) |
| Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis | (Orphanet:171839) |
| Crigler-Najjar syndrome | (Orphanet:205) |
| Crigler-Najjar syndrome type 1 | (Orphanet:79234) |
| Familial Mediterranean fever | (Orphanet:342) |
| Floating-Harbor syndrome | (Orphanet:2044) |
| Free sialic acid storage disease | (Orphanet:834) |
| Fucosidosis | (Orphanet:349) |
| Galactosemia | (Orphanet:352) |
| Glutaryl-CoA dehydrogenase deficiency | (Orphanet:25) |
| Growth hormone insensitivity syndrome | (Orphanet:181393) |
| Hereditary cerebral hemorrhage with amyloidosis, Piedmont type | (Orphanet:324703) |
| Hereditary folate malabsorption | (Orphanet:90045) |
| Hereditary neuropathy with liability to pressure palsies | (Orphanet:640) |
| Holoprosencephaly | (Orphanet:2162) |
| Hurler syndrome | (Orphanet:93473) |
| Hydrocephaly - tall stature - joint laxity | (Orphanet:2181) |
| Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
| Idiopathic juvenile osteoporosis | (Orphanet:85193) |
| Incontinentia pigmenti | (Orphanet:464) |
| Infant botulism | (Orphanet:178478) |
| Intellectual deficit, X-linked, Pai type | (Orphanet:85322) |
| Intestinal botulism | (Orphanet:178481) |
| Isolated spina bifida | (Orphanet:823) |
| Juvenile amyotrophic lateral sclerosis | (Orphanet:300605) |
| Juvenile primary lateral sclerosis | (Orphanet:247604) |
| Keratoderma hereditarium mutilans with ichthyosis | (Orphanet:79395) |
| Krabbe disease | (Orphanet:487) |
| L-2-hydroxyglutaric aciduria | (Orphanet:79314) |
| Laron syndrome | (Orphanet:633) |
| Lesch-Nyhan syndrome | (Orphanet:510) |
| Metachromatic leukodystrophy | (Orphanet:512) |
| Microphthalmia with linear skin defects syndrome | (Orphanet:2556) |
| Mild Canavan disease | (Orphanet:314918) |
| Moebius syndrome | (Orphanet:570) |
| Neuroferritinopathy | (Orphanet:157846) |
| Neurogenic thoracic outlet syndrome | (Orphanet:100073) |
| Non-polyposis Turcot syndrome | (Orphanet:99817) |
| O'Sullivan-McLeod syndrome | (Orphanet:99965) |
| Oculo-palato-cerebral syndrome | (Orphanet:2714) |
| Pelizaeus-Merzbacher disease | (Orphanet:702) |
| Pyruvate dehydrogenase deficiency | (Orphanet:765) |
| Rabies | (Orphanet:770) |
| Riboflavin transporter deficiency | (Orphanet:97229) |
| Sandhoff disease | (Orphanet:796) |
| Severe Canavan disease | (Orphanet:314911) |
| Spastic paraplegia type 2 | (Orphanet:99015) |
| Sturge-Weber syndrome | (Orphanet:3205) |
| Thoracic outlet syndrome | (Orphanet:97330) |
| Trisomy 20p | (Orphanet:261318) |
| Von Hippel-Lindau disease | (Orphanet:892) |
| Waardenburg syndrome type 3 | (Orphanet:896) |
| Waldenström macroglobulinemia | (Orphanet:33226) |
| 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 intellectual deficit - cerebellar hypoplasia | (Orphanet:137831) |