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Diseases

Angiodysplasia

angiodysplasia

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
Angiodysplasia
Standard Disease Name
angiodysplasia
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
C565118
OMIM ID
125230
UMLS ID
C1852278
HPO ID
No data

Description and Extensions

Description
SNOMEDCT_US_2016_09_01:This syndrome has characteristics of the association of congenital hearing loss and facial dysmorphism (facial asymmetry, a broad nasal root and small nasal alae). It has been described in two members (father and daughter) of one Jewish family. Temporal alopecia was also noted. Transmission appeared to be autosomal dominant.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
04
HIF1A
hypoxia inducible factor 1 subunit alpha
hypoxia inducible factor 1 subunit alpha
05
PTPRF
protein tyrosine phosphatase receptor type F
protein tyrosine phosphatase receptor type F
07
VEGFA
vascular endothelial growth factor A
vascular endothelial growth factor A