LH resistance due to partial LH receptor inactivation (Q104178): Difference between revisions
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Revision as of 10:03, 17 August 2026
This is a rare autosomal recessive genetic and endocrine syndrome, characterised by an inability of the body to respond to luteinizing hormone (LH), a gonadotropin which is normally responsible for signalling Leydig cells of the testicles to produce testos. This diagnosis is due to partial LH receptor inactivation.
| Language | Label | Description | Also known as |
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| default for all languages | ID_74297048 |
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| English | LH resistance due to partial LH receptor inactivation |
This is a rare autosomal recessive genetic and endocrine syndrome, characterised by an inability of the body to respond to luteinizing hormone (LH), a gonadotropin which is normally responsible for signalling Leydig cells of the testicles to produce testos. This diagnosis is due to partial LH receptor inactivation. |
Statements
CID11:ID_74297048
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