Autosomal recessive spastic paraplegia type 23 (Q99390): Difference between revisions
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Revision as of 16:03, 16 August 2026
Progressive spastic paraplegia associated with the SPG23 phenotype that is characterized by by peripheral neuropathy, skin pigment abnormalities, premature graying of hair and characteristic facial features.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1595722974 |
||
| English | Autosomal recessive spastic paraplegia type 23 |
Progressive spastic paraplegia associated with the SPG23 phenotype that is characterized by by peripheral neuropathy, skin pigment abnormalities, premature graying of hair and characteristic facial features. |
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CID11:ID_1595722974
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dki-india-ID_1595722974
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