Autosomal dominant hereditary disorder
Brachydactyly
Congenital anomaly of finger
Congenital anomaly of skeletal bone
Congenital deformity of hand
Congenital musculoskeletal deformity
Deformity of bone
Developmental hereditary disorder
Finding of bone in hand
Finding of musculoskeletal structure of finger
Hereditary disorder of musculoskeletal system
Longitudinal deficiency of bone
Longitudinal deficiency of part of upper limb
Reduction deformity of finger
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Brachydactyly type A3 (disorder)
Brachydactyly type A3
A congenital malformation characterized by shortening of the middle phalanx of the fifth finger. Inherited as an autosomal dominant trait.
brachydactylie type A3
Id890438002
StatusPrimitive
Associated morphologyAbnormally short growth
Finding siteStructure of middle phalanx of little finger
OccurrenceCongenital
Pathological processPathological developmental process
ICD-10 complex map reference set
TargetQ71.8
RuleTRUE
AdviceALWAYS Q71.8
CorrelationSNOMED CT source code to target map code correlation not specified