Congenital hearing impairment (Q42156): Difference between revisions

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+August 2026Timestamp +2026-08-13T00:00:00Z
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@@ Property / Linked ICD 10 @@
+H90-H95
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Latest revision as of 08:34, 13 August 2026

Both dominant and recessive genes exist which can cause mild to profound impairment. If a family has a dominant gene for deafness it will persist across generations because it will manifest itself in the offspring even if it is inherited from only one parent. If a family had genetic hearing impairment caused by a recessive gene it will not always be apparent as it will have to be passed onto offspring from both parents. Hearing impairment is sustained before the acquisition of language, which occurs due to a congenital condition.

Language	Label	Description	Also known as
default for all languages	AB50
English	Congenital hearing impairment	Both dominant and recessive genes exist which can cause mild to profound impairment. If a family has a dominant gene for deafness it will persist across generations because it will manifest itself in the offspring even if it is inherited from only one parent. If a family had genetic hearing impairment caused by a recessive gene it will not always be apparent as it will have to be passed onto offspring from both parents. Hearing impairment is sustained before the acquisition of language, which occurs due to a congenital condition.