Disease Browser
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Parent Node: Intellectual Disability (D008607) | Parent Node: Muscular Atrophy, Spinal (D009134) | ..Starting node ..Spinal Muscular Atrophy with Mental Retardation (C564807)
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Sister Nodes: | ..Bulbo-Spinal Atrophy, X-Linked (D055534) 1
| ..Camptocormia (C537968)
| ..Distal Hereditary Motor Neuropathy, Type II (C580044)
| ..Neuronopathy, Distal Hereditary Motor, Type I (C566675)
| ..Neuronopathy, Distal Hereditary Motor, Type IIB (C567084)
| ..Neuronopathy, Distal Hereditary Motor, Type V (C563443)
| ..Neuronopathy, Distal Hereditary Motor, Type Viib (C564362)
| ..Neuropathy, Distal Hereditary Motor, Type IIA (C563561)
| ..Neuropathy, Distal Hereditary Motor, Type VIIA (C563562)
| ..SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY (OMIM:181405)
| ..Scapuloperoneal Syndrome, Neurogenic, Kaeser Type (C566695)
| ..Spinal Muscular Atrophies of Childhood (D014897) 7
| ..Spinal muscular atrophy 4 (C538417)
| ..Spinal Muscular Atrophy with Mental Retardation (C564807)
| ..Spinal muscular atrophy with respiratory distress 1 (C536880)
| ..Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 (C564626)
| ..Spinal Muscular Atrophy, Distal, Congenital Nonprogressive (C563981)
| ..Spinal Muscular Atrophy, Distal, X-Linked 3 (C564506)
| ..Spinal Muscular Atrophy, Facioscapulohumeral Type (C566674)
| ..Spinal muscular atrophy, Jerash type (C535715)
| ..Spinal Muscular Atrophy, Late-Onset, Finkel Type (C566673)
| ..Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant (C566672)
| ..Spinal muscular atrophy, Ryukyuan type (C536881)
| ..Spinal Muscular Atrophy, Segmental (C566670)
| ..Spinal Muscular Atrophy, Type IV (C563948)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 10485 |
Name: | Spinal Muscular Atrophy with Mental Retardation |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D008607|MESH:D009134 |
TreeNumbers: | C10.228.854.468/C564807 |C10.574.562.500/C564807 |C10.597.606.643/C564807 |C10.668.467.500/C564807 |C10.668.475/C564807 |C23.888.592.604.646/C564807 |F03.550.600/C564807 |
Synonyms: | |
Slim Mappings: | Mental disorder|Nervous system disease|Signs and symptoms |
Reference: |
MedGen: C564807
MeSH: C564807
OMIM: 271109;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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