Auditory system hereditary disorder	Autosomal dominant hereditary disorder	Conductive hearing loss	Congenital anomaly of ear with impairment of hearing	Congenital micrognathism	Developmental hereditary disorder	Hereditary disorder of musculoskeletal system	Microtia	Multiple malformation syndrome with facial defects as major feature
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Thickened earlobe with conductive deafness syndrome (disorder)
	Thickened earlobe with conductive deafness syndrome
	Escher Hirt syndrome
	Syndrome with characteristics of microtia with thickened ear lobes, micrognathia and conductive hearing loss due to congenital ossicular anomalies. It has been described in two families. The mode of inheritance is autosomal dominant.
	syndroom van verdikte oorlellen en conductief gehoorverlies
	syndroom van verdikte oorlellen en geleidingsgehoorverlies syndroom van Escher-Hirt

Id	722476007
Status	Primitive

Interprets

Associated morphology	Hypoplasia
Finding site	Bone structure of mandible
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Congenital smallness
Finding site	External ear structure
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	H90.0
Rule	TRUE
Advice	ALWAYS H90.0 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified