Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandKyphosis (D007738)
Parent Node:
expandSpinal Osteochondrosis (D055035)
..Starting node
..expandScheuermann Disease (D012544)

       Child Nodes:



 Sister Nodes: 
..expandScheuermann Disease (D012544)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:10014
Name:Scheuermann Disease
Definition:A type of juvenile osteochondrosis affecting the fibrocartilaginous disc (INTERVERTEBRAL DISC) in the thoracic or thoracolumbar region of the SPINE. It is characterized by a forward concave SPINAL CURVATURE or KYPHOSIS.
Alternative IDs:OMIM:181440
ParentIDs:MESH:D007738|MESH:D055035
TreeNumbers:C05.116.821.500.500 |C05.116.900.800.500.500 |C05.116.900.808.500
Synonyms:Adolescent Kyphoses |Adolescent Kyphosis |Juvenile Kyphoses |Juvenile Kyphoses, Scheuermann |Juvenile Kyphosis |Juvenile Kyphosis, Scheuermann |Juvenile Osteochondrosis of Spine |Kyphoses, Adolescent |Kyphoses, Juvenile |Kyphoses, Scheuermann |Kyphoses, Scheuerman
Slim Mappings:Musculoskeletal disease
Reference: MedGen: D012544
MeSH: D012544
OMIM: 181440;

Genes:
Phenotypes
1 HP:0000006Autosomal dominant inheritance
2 HP:0002808Kyphosis
3 HP:0010891Morbus Scheuermann
Disease Causing ClinVar Variants