Disease Browser
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Parent Node: Ataxia (D001259) | Parent Node: Intellectual Disability (D008607) | Parent Node: Paraplegia (D010264) | ..Starting node ..Spastic Paraplegia, Ataxia, And Mental Retardation (C564378)
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Sister Nodes: | ..Brown-Sequard Syndrome (D018437)
| ..Fryns Macrocephaly (C563963)
| ..Mental Retardation with Spastic Paraplegia (C564099)
| ..Optic Atrophy Spastic Paraplegia Syndrome (C564084)
| ..Spastic Paraplegia 24, Autosomal Recessive (C564375)
| ..Spastic Paraplegia 28, Autosomal Recessive (C563732)
| ..Spastic Paraplegia 30, Autosomal Recessive (C563677)
| ..Spastic Paraplegia Type 11 (C580453)
| ..Spastic Paraplegia Type 3a (C580455)
| ..Spastic Paraplegia Type 4 (C580456)
| ..Spastic Paraplegia Type 7 (C580457)
| ..Spastic Paraplegia Type 8 (C580458)
| ..Spastic Paraplegia, Ataxia, And Mental Retardation (C564378)
| ..Spastic Paraplegia, Optic Atrophy, and Neuropathy (C563702)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 10403 |
Name: | Spastic Paraplegia, Ataxia, And Mental Retardation |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D001259|MESH:D008607|MESH:D010264 |
TreeNumbers: | C10.597.350.090/C564378 |C10.597.606.643/C564378 |C10.597.622.669/C564378 |C23.888.592.350.090/C564378 |C23.888.592.604.646/C564378 |C23.888.592.636.637/C564378 |F03.550.600/C564378 |
Synonyms: | |
Slim Mappings: | Mental disorder|Nervous system disease|Signs and symptoms |
Reference: |
MedGen: C564378
MeSH: C564378
OMIM: 607565;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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