KEGG   DISEASE: Prepubertal periodontitis
Entry
H02050                      Disease                                
Name
Prepubertal periodontitis
Description
Prepubertal periodontitis (PPP) is a rare and rapidly progressive disease of young children that results in destruction of the periodontal support of the primary dentition. Both autosomal dominant and recessive forms have been reported for PPP. Mutations in cathepsin C gene cause this disease.
Category
Digestive system disease
Brite
Human diseases in ICD-11 classification [BR:br08403]
 13 Diseases of the digestive system
  Diseases or disorders of orofacial complex
   DA0C  Periodontal disease
    H02050  Prepubertal periodontitis
Pathway
hsa04142  Lysosome
hsa04210  Apoptosis
Gene
CTSC [HSA:1075] [KO:K01275]
Other DBs
ICD-11: DA0C.1
MeSH: D010518
OMIM: 170650
Reference
  Authors
Hart TC, Hart PS, Michalec MD, Zhang Y, Marazita ML, Cooper M, Yassin OM, Nusier M, Walker S
  Title
Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutation.
  Journal
J Med Genet 37:95-101 (2000)
DOI:10.1136/jmg.37.2.95
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