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Multiple epiphyseal dysplasia Lowry type (disorder)
Multiple epiphyseal dysplasia Lowry type
Multiple epiphyseal dysplasia with Robin phenotype
A rare primary bone dysplasia with characteristics of small, flat epiphyses (especially the capital femoral epiphyses), rhizomelic shortening of limbs, cleft of secondary palate, micrognathia, mild joint contractures and facial dysmorphism (including mildly upward-slanting palpebral fissures, hypertelorism, broad nasal tip). Additionally reported features include scoliosis, genu valgum, mild pectus excavatum, platyspondyly, dislocated radial heads, brachydactyly, hypoplastic fibulae and talipes equinovarus.
multipele epifysaire dysplasie Lowry-type
meervoudige epifysaire dysplasie met Robin-fenotype
meervoudige epifysaire dysplasie type Lowry
Id768935003
StatusPrimitive
Associated morphologyDysplasia
Finding siteStructure of epiphysis
OccurrenceCongenital
Pathological processPathological developmental process
Clinical courseProgressive
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetQ78.8
RuleTRUE
AdviceALWAYS Q78.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified