LH resistance due to complete LH receptor inactivation (Q104184)
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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 complete LH receptor inactivation.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_232167901 |
||
| English | LH resistance due to complete 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 complete LH receptor inactivation. |
Statements
CID11:ID_232167901
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dki-india-ID_232167901
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Concluído
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16 August 2026
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