Cerebral palsy

Symptom Information:

Symptom ID: HPO:0100021
Synonyms:
Cerebral paralysis [HPO:0100021]
Cerebral paralysis [Orphanet:43380]
Cerebral palsy [OMIM:Cerebral palsy]
Acute palsy [Orphanet:43380]
Cerebral palsy [MedDRA:10008129]
Quality:
Cross references:
Orphanet:43380 "Acute palsy" [Orphanet:43380]
OMIM: "Cerebral palsy" [OMIM:Cerebral palsy]
Is a (Direct Parents):
MedDRA Cerebral disorders congenital
HPO         Abnormality of central motor function
HPO         Abnormality of movement
Orphanet [DEL]Motor deficit/trouble
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 movement(HPO:0100022)
                Cerebral palsy(HPO:0100021)
             Abnormality of central motor function(HPO:0011442)
                Cerebral palsy(HPO:0100021)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Neurological disorders congenital(MedDRA:10029299)
       Cerebral disorders congenital(MedDRA:10052634)
          Cerebral palsy(HPO:0100021)
Database Frequency: 36 / 7739
Resource:

All diseases associated with this symptom:

Acromegaly (Orphanet:963)
Adult intestinal botulism (Orphanet:178487)
Aldosterone-producing adenoma with seizures and neurological abnormalities (Orphanet:369929)
Atypical teratoid tumor (Orphanet:99966)
Botulism (Orphanet:1267)
CEREBRAL PALSY, ATAXIC, AUTOSOMAL RECESSIVE (OMIM:605388)
CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 2 (OMIM:612900)
DYSMYELINATION WITH JAUNDICE (OMIM:224250)
Foodborne botulism (Orphanet:228371)
Hurler syndrome (Orphanet:93473)
Hyperkalemic periodic paralysis (Orphanet:682)
Hypocomplementemic urticarial vasculitis (Orphanet:36412)
Iatrogenic botulism (Orphanet:254509)
Infant botulism (Orphanet:178478)
Inhalational botulism (Orphanet:254504)
Inherited congenital spastic tetraplegia (Orphanet:210141)
Locked-in syndrome (Orphanet:2406)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 26 (OMIM:615834)
Maffucci syndrome (Orphanet:163634)
Ornithine transcarbamylase deficiency (Orphanet:664)
Pachydermoperiostosis (Orphanet:2796)
Porphyria (Orphanet:738)
Porphyria cutanea tarda (Orphanet:101330)
Porphyria due to ALA dehydratase deficiency (Orphanet:100924)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
Pyruvate dehydrogenase deficiency (Orphanet:765)
Rabies (Orphanet:770)
Rhabdoid tumor (Orphanet:69077)
SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE (OMIM:614067)
Scheie syndrome (Orphanet:93474)
Severe intellectual deficit and progressive spastic paraplegia (Orphanet:280763)
TENORIO SYNDROME (OMIM:616260)
Toxin-mediated infectious botulism (Orphanet:230800)
Transient familial neonatal hyperbilirubinemia (Orphanet:2312)
Wound botulism (Orphanet:178475)
Wyburn-Mason syndrome (Orphanet:53719)