OMOP Concept 192606
Paraplegia
StandardConditionSNOMED60389000Disorder
Maps from
25
Descendants
112
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
25 source codes normalize to Paraplegia via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Paraplegia across source vocabularies.
- Lower paraplegia
- parálisis de ambas extremidades inferiores
- parálisis de ambos miembros inferiores
- Paralysis of both lower limbs
- Paraplegia (complete or partial paralysis of legs)
- Paraplegia (disorder)
- paraplejía
- paraplejía inferior
- paraplejía (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(19)Roll up to these when you need a wider cohort.
- 1Bilateral lower limb paralytic syndrome
- 1Complete bilateral paralysis
- 2Disorder of left lower extremity
- 2Disorder of nervous system
- 2Disorder of right lower extremity
- 2Paralytic syndrome
- 3Disorder of body system
- 3Disorder of lower limb
- 3Movement disorder
- 3Paralysis
- 4Disease
- 4Disorder of limb
- 4Finding of lower limb
- 4Finding of movement
- 4Motor dysfunction
- 5Clinical finding
- 5Finding of limb structure
- 5Motor nervous system finding
- 6Neurological finding
Narrower concepts
(112)Included automatically when you query with descendants.
- 1Acute paraplegia
- 1Cerebral paraplegia
- 1Chronic paraplegia
- 1Complete paraplegia
- 1Congenital paraplegia
- 1Flaccid paraplegia
- 1Incomplete paraplegia
- 1Paraplegia as sequela of cerebrovascular accident
- 1Paraplegia with neurogenic urinary bladder
- 1Spastic paraplegia
- 1Spinal paraplegia
- 2Athetosis with spastic paraplegia
- 2Hereditary spastic paraplegia
- 2Macrocephaly, short stature, paraplegia syndrome
- 2Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome
- 3Autosomal dominant hereditary spastic paraplegia
- 3Autosomal recessive hereditary spastic paraplegia
- 3Autosomal spastic paraplegia type 30
- 3Complicated hereditary spastic paraplegia
- 3Pure hereditary spastic paraplegia
- 3X-linked hereditary spastic paraplegia
- 4Allan-Herndon-Dudley syndrome
- 4Autosomal dominant complex hereditary spastic paraplegia
- 4Autosomal dominant spastic paraplegia type 10
- 4Autosomal dominant spastic paraplegia type 12
- 4Autosomal dominant spastic paraplegia type 13
- 4Autosomal dominant spastic paraplegia type 19
- 4Autosomal dominant spastic paraplegia type 3
- 4Autosomal dominant spastic paraplegia type 31
- 4Autosomal dominant spastic paraplegia type 37
- 4Autosomal dominant spastic paraplegia type 4
- 4Autosomal dominant spastic paraplegia type 41
- 4Autosomal dominant spastic paraplegia type 42
- 4Autosomal dominant spastic paraplegia type 6
- 4Autosomal dominant spastic paraplegia type 73
- 4Autosomal dominant spastic paraplegia type 8
- 4Autosomal dominant spastic paraplegia type 9B
- 4Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction
- 4Autosomal recessive spastic paraplegia type 11
- 4Autosomal recessive spastic paraplegia type 14
- 4Autosomal recessive spastic paraplegia type 15
- 4Autosomal recessive spastic paraplegia type 18
- 4Autosomal recessive spastic paraplegia type 21
- 4Autosomal recessive spastic paraplegia type 23
- 4Autosomal recessive spastic paraplegia type 24
- 4Autosomal recessive spastic paraplegia type 25
- 4Autosomal recessive spastic paraplegia type 26
- 4Autosomal recessive spastic paraplegia type 27
- 4Autosomal recessive spastic paraplegia type 28
- 4Autosomal recessive spastic paraplegia type 32
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