Skip to main content
Diseases

Plummer Vinson Syndrome

plummer vinson syndrome

Entity Type
Diseases
Relation Groups
1
Relation Preview
2

Basic Information

Grouped by core information, identifiers, and descriptions.

Quick relations do not expand inferred candidates by default. Load path-derived ingredients or herbs when needed.

Core Information

Disease Name
Plummer Vinson Syndrome
Standard Disease Name
plummer vinson syndrome
MeSH Tree
No data
ICD-10
D50.1

Identifiers

DO ID
No data
MeSH ID
D011004
OMIM ID
No data
UMLS ID
C0032249
HPO ID
No data

Description and Extensions

Description
NCI2016_NCI-GLOSS_1602D:A disorder marked by anemia caused by iron deficiency, and a web-like growth of membranes in the throat that makes swallowing difficult. Having Plummer-Vinson syndrome may increase the risk of developing esophageal cancer.|NCI2016_02D:A syndrome characterized by dysphagia, upper esophageal webs, iron deficiency anemia, and glossitis.|MSH2017_2016_08_12:A syndrome of DYSPHAGIA with IRON-DEFICIENCY ANEMIA that is due to congenital anomalies in the ESOPHAGUS (such as cervical esophageal webs). It is known as Patterson-Kelly syndrome in the United Kingdom.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease2 Targets
02
RBBP8
RB binding protein 8, endonuclease
RB binding protein 8, endonuclease