Auditory system hereditary disorder
Autosomal dominant hereditary spastic paraplegia
Chronic disease of ear
Chronic disease of genitourinary system
Chronic nephropathy
Complicated hereditary spastic paraplegia
Congenital nephropathy
Congenital neurological disorder
Congenital sensorineural hearing loss
Decreased hearing
Disorder of sensory function
Hearing loss associated with syndrome
Hereditary nephropathy
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Spastic paraplegia, nephritis, deafness syndrome (disorder)
Spastic paraplegia, nephritis, deafness syndrome
Fitzsimmons Walson Mellor syndrome
Syndrome with characteristics of variable spastic paraplegia, bilateral sensorineural deafness, intellectual deficit and progressive nephropathy. It has been described in six members of a family.
syndroom van spastische paraplegie, nefritis en doofheid
Id733089005
StatusPrimitive
Has interpretationDecreased
InterpretsHearing
Finding siteKidney structure
OccurrenceCongenital
Finding siteEar structure
OccurrenceCongenital
Associated morphologyDegenerative abnormality
Finding siteSpinal cord structure
Clinical courseProgressive
Finding siteLower limb structure
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetG11.4
RuleTRUE
AdviceALWAYS G11.4 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
TargetN07.9
RuleTRUE
AdviceALWAYS N07.9
CorrelationSNOMED CT source code to target map code correlation not specified
TargetH90.3
RuleTRUE
AdviceALWAYS H90.3
CorrelationSNOMED CT source code to target map code correlation not specified