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Diseases

Dyschromatosis universalis hereditaria

dyschromatosis universalis hereditaria

Entity Type
Diseases
Relation Groups
3
Relation Preview
24

Basic Information

Grouped by core information, identifiers, and descriptions.

Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.

Core Information

Disease Name
Dyschromatosis universalis hereditaria
Standard Disease Name
dyschromatosis universalis hereditaria
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
No data
OMIM ID
No data
UMLS ID
C1335486
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:A non-keratinizing or keratinizing squamous cell carcinoma that arises centrally from the jaw. It is characterized by a solid pattern, infiltration of the marrow spaces, and osseous resorption.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
02
ADAR
adenosine deaminase RNA specific
adenosine deaminase RNA specific
04
CREB1
cAMP responsive element binding protein 1
cAMP responsive element binding protein 1
05
MAP2K2
mitogen-activated protein kinase kinase 2
mitogen-activated protein kinase kinase 2
06
MAPK3
mitogen-activated protein kinase 3
mitogen-activated protein kinase 3