| Disease Browser
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Parent Node:
 Spinal Curvatures (D013121) | ..Starting node
.. Scoliosis (D012600)
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Child Nodes:
| | ........Acrodysplasia scoliosis (C538180) | | ........Cervical Hypertrichosis with Underlying Kyphoscoliosis (C566142) | | ........Coffin syndrome 1 (C536435) | | ........Daish Hardman Lamont syndrome (C535770) | | ........Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, And Mental Retardation (C566408) | | ........Gaze Palsy, Familial Horizontal, with Progressive Scoliosis (C564593) | | ........Iida Kannari syndrome (C536284) | | ........Kyphoscoliosis 1 (C565711) | | ........Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis (C567770) | | ........Omphalocele exstrophy imperforate anus (C537748) | | ........Parastremmatic dwarfism (C537172) | | ........Pilotto syndrome (C537400) | | ........Prata Libéral Gonçalves syndrome (C538277) | | ........Rhizomelic dysplasia, scoliosis, and retinitis pigmentosa (C537610) | | ........Rigid spine syndrome (C535683) | | ........Scoliosis, Arachnodactyly, And Blindness (C567309) | | ........SCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 1 (OMIM:181800) | | ........SCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 2 (OMIM:607354) | | ........SCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 3 (OMIM:608765) | | ........SCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 4 (OMIM:612238) | | ........SCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 5 (OMIM:612239) | | ........Shprintzen omphalocele syndrome (C537329) | | ........Spondylocarpotarsal synostosis (C535780) | | ........Tsukahara Syndrome (C566376) | | ........Waaler Aarskog syndrome (C536461) |
Sister Nodes: | ..Camptocormia (C537968)
| ..Kyphosis (D007738)  11
| ..Lordosis (D008141) 2
| ..Scoliosis (D012600) 25
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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| Term ID: | 10069 |
| Name: | Scoliosis |
| Definition: | An appreciable lateral deviation in the normally straight vertical line of the spine. (Dorland, 27th ed) |
| Alternative IDs: | |
| ParentIDs: | MESH:D013121 |
| TreeNumbers: | C05.116.900.800.875 |
| Synonyms: | Scolioses |
| Slim Mappings: | Musculoskeletal disease |
| Reference: |
MedGen: D012600
MeSH: D012600
OMIM:
Genes: | | Phenotypes | | | Disease Causing ClinVar Variants | |
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