Congenital micrognathism
Developmental hereditary disorder
Hereditary disorder of musculoskeletal system
Holoprosencephaly sequence
Multiple malformation syndrome with facial defects as major feature
|||||
Agnathia, holoprosencephaly, situs inversus syndrome (disorder)
Agnathia, holoprosencephaly, situs inversus syndrome
An extremely rare and fatal association syndrome with characteristics of absence of the mandible, cerebral malformations with facial anomalies related to a defect in cleavage in the embryonic brain (e.g. synophthalmia, malformed and low-set ears fused in midline, agenesis of the olfactory bulbs, microstomia, hypoglossia/aglossia) and situs inversus partialis or totalis.
syndroom van agenesie van kaak, holoprosencefalie en situs inversus
syndroom van agnathie, holoprosencefalie en situs inversus
Id722283003
StatusPrimitive
Associated morphologyHypoplasia
Finding siteBone structure of mandible
OccurrenceCongenital
Pathological processPathological developmental process
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetQ87.0
RuleTRUE
AdviceALWAYS Q87.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified