Abnormality of central motor function

Symptom Information:

Symptom ID: HPO:0011442
Cross references:
Is a (Direct Parents):
HPO         Abnormality of nervous system physiology
Is a (Whole tree): HPO:
    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)
Database Frequency: 76 / 7739

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)