Autosomal hereditary disorder
Congenital malformation syndromes associated with short stature
Developmental hereditary disorder
Hereditary disorder of musculoskeletal system
Spondylodysplastic group
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Brachyolmia (disorder)
Brachyolmia
brachyolmie
Id
254088006
Status
Primitive
Associated morphology
Dysplasia
Finding site
Bone structure
Occurrence
Congenital
Pathological process
Pathological developmental process
Interprets
Height / growth measure
ICD-10 complex map reference set
Target
Q78.8
Rule
TRUE
Advice
ALWAYS Q78.8
Correlation
SNOMED CT source code to target map code correlation not specified
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Autosomal dominant brachyolmia
Autosomal recessive brachyolmia
Brachyolmia - Maroteaux type
Verloes Bourguignon syndrome