Preferred Name |
Cerebral Palsy |
Synonyms |
Cerebral Palsy, Monoplegic, Infantile |
Definitions |
A heterogeneous group of nonprogressive motor disorders caused by chronic brain injuries that originate in the prenatal period, perinatal period, or first few years of life. The four major subtypes are spastic, athetoid, ataxic, and mixed cerebral palsy, with spastic forms being the most common. The motor disorder may range from difficulties with fine motor control to severe spasticity (see MUSCLE SPASTICITY) in all limbs. Spastic diplegia (Little disease) is the most common subtype, and is characterized by spasticity that is more prominent in the legs than in the arms. Pathologically, this condition may be associated with LEUKOMALACIA, PERIVENTRICULAR. (From Dev Med Child Neurol 1998 Aug;40(8):520-7) |
ID |
http://purl.bioontology.org/ontology/MESH/D002547 |
altLabel |
Cerebral Palsy, Monoplegic, Infantile Monoplegic Infantile Cerebral Palsy Cerebral Palsy, Dyskinetic Cerebral Palsy, Rolandic Type Cerebral Palsy, Hypotonic Cerebral Palsy, Dystonic Rigid Hypotonic Cerebral Palsy Infantile Cerebral Palsy, Quadriplegic Dystonic-Rigid Cerebral Palsy Little Disease Diplegic Infantile Cerebral Palsy Infantile Cerebral Palsy, Monoplegic Cerebral Palsy, Dystonic-Rigid Atonic Cerebral Palsy Cerebral Palsy, Congenital Spastic Diplegia Spastic Diplegias Diplegia, Spastic Cerebral Palsies, Athetoid Monoplegic Cerebral Palsies Monoplegic Cerebral Palsy Cerebral Palsy, Atonic Cerebral Palsy, Diplegic, Infantile CP (Cerebral Palsy) Infantile Cerebral Palsy, Diplegic Spastic Cerebral Palsies Mixed Cerebral Palsies Cerebral Palsy, Quadriplegic, Infantile Little's Disease Dystonic-Rigid Cerebral Palsies Cerebral Palsies, Dystonic-Rigid Hypotonic Cerebral Palsies Quadriplegic Infantile Cerebral Palsy Spastic Cerebral Palsy Mixed Cerebral Palsy Diplegias, Spastic Cerebral Palsies, Dyskinetic Cerebral Palsy, Monoplegic Cerebral Palsy, Spastic Dyskinetic Cerebral Palsy Cerebral Palsy, Athetoid Cerebral Palsies, Monoplegic Athetoid Cerebral Palsy Rolandic Type Cerebral Palsy Cerebral Palsy, Mixed Congenital Cerebral Palsy |
AN |
do not index under MUSCLE SPASTICITY unless especially discussed & then only NIM |
AQL |
BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI |
cui |
C0270742 C0553767 C0007789 C0154697 C0338596 C0394007 C0394003 C0023882 C0270807 C0751024 C0154695 C0154698 C0751025 |
DC |
1 |
definition |
A heterogeneous group of nonprogressive motor disorders caused by chronic brain injuries that originate in the prenatal period, perinatal period, or first few years of life. The four major subtypes are spastic, athetoid, ataxic, and mixed cerebral palsy, with spastic forms being the most common. The motor disorder may range from difficulties with fine motor control to severe spasticity (see MUSCLE SPASTICITY) in all limbs. Spastic diplegia (Little disease) is the most common subtype, and is characterized by spasticity that is more prominent in the legs than in the arms. Pathologically, this condition may be associated with LEUKOMALACIA, PERIVENTRICULAR. (From Dev Med Child Neurol 1998 Aug;40(8):520-7) |
DX |
19660101 |
Inverse of AQ |
http://purl.bioontology.org/ontology/MESH/Q000401 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000523 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000652 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000151 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000209 |
Mapped from |
http://purl.bioontology.org/ontology/MESH/C537945 http://purl.bioontology.org/ontology/MESH/C565587 http://purl.bioontology.org/ontology/MESH/C567858 http://purl.bioontology.org/ontology/MESH/C536143 http://purl.bioontology.org/ontology/MESH/C567853 http://purl.bioontology.org/ontology/MESH/C565610 http://purl.bioontology.org/ontology/MESH/C538101 http://purl.bioontology.org/ontology/MESH/C537761 |
MDA |
19990101 |
MMR |
20030725 |
MN |
C10.228.140.140.254 |
notation |
D002547 |
prefLabel |
Cerebral Palsy |
TERMUI |
T367028 T367026 T367046 T367027 T367044 T367009 T367030 T367031 T007419 T367010 T367035 T367045 T367036 T367034 T007423 T367043 T367008 T367049 T367047 T367011 T007420 T367048 T367032 T367029 T367033 T007421 T367050 |
TH |
UNK (19XX) NLM (2000) NLM (1966) NLM (1995) |
tui |
T019 T047 |
subClassOf |