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Diseases

Hereditary Gingival Fibromatosis

hereditary gingival fibromatosis

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Hereditary Gingival Fibromatosis
Standard Disease Name
hereditary gingival fibromatosis
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D050815
OMIM ID
MTHU052627
UMLS ID
C0521169
HPO ID
No data

Description and Extensions

Description
NCI2016_NCI-GLOSS_1602D:A type of break in a bone caused by pressure and in which the bone collapses. Compression fractures usually occur in the spine (backbone) and in bones made weak by cancer or by osteoporosis (a decrease in bone mass and density).|MSH2017_2016_08_12:Crumbling or smashing of cancellous BONE by forces acting parallel to the long axis of bone. It is applied particularly to vertebral body fractures (SPINAL FRACTURES). (Blauvelt and Nelson, A Manual of Orthopedic Terminology, 1994, p4)
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
05
ICAM1
intercellular adhesion molecule 1
intercellular adhesion molecule 1
06
PIK3R1
phosphoinositide-3-kinase regulatory subunit 1
phosphoinositide-3-kinase regulatory subunit 1
07
SOCS1
suppressor of cytokine signaling 1
suppressor of cytokine signaling 1
08
SOS1
SOS Ras/Rac guanine nucleotide exchange factor 1
SOS Ras/Rac guanine nucleotide exchange factor 1