| Disease Browser
|
Parent Node:
 Kyphosis (D007738) | Parent Node:
Scoliosis (D012600) | ..Starting node
.. Kyphoscoliosis 1 (C565711)
|
Child Nodes:
|
Sister 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)
|
Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
|
|
|
| Term ID: | 6156 |
| Name: | Kyphoscoliosis 1 |
| Definition: | |
| Alternative IDs: | OMIM:610170 |
| ParentIDs: | MESH:D007738|MESH:D012600 |
| TreeNumbers: | C05.116.900.800.500/C565711 |C05.116.900.800.875/C565711 |
| Synonyms: | KYPSC1 |
| Slim Mappings: | Musculoskeletal disease |
| Reference: |
MedGen: C565711
MeSH: C565711
OMIM: 610170;
Genes: | | Phenotypes | | | Disease Causing ClinVar Variants | |
|
