Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026
Id http://purl.bioontology.org/ontology/OMIM/620207
http://purl.bioontology.org/ontology/OMIM/620207
Preferred Name

BLOOD GROUP, ER
Synonyms
ER
ER BLOOD GROUP SYSTEM
Type http://www.w3.org/2002/07/owl#Class

All Properties

altLabel
ER
ER BLOOD GROUP SYSTEM
prefLabel
BLOOD GROUP, ER
Gene Symbol
MIB
DHS
PIEZO1
FAM38A
ER
LMPHM6
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Scope Statement
Caused by mutation in the PIEZO1-type mechanosensitive ion channel component 1 gene (PIEZO1, 611184.0017) [MOLECULAR BASIS]
Anti-Er(4) and anti-Er(5) have been associated with hemolysis and fetal hydrops in utero [MISCELLANEOUS]
Most individuals with anti-Er-alloantibodies do not have significant clinical manifestations [MISCELLANEOUS]
type
Has manifestation
tui
T022
Gene Locus
16q24.3
MIMTYPEMEANING
Phenotype description, molecular basis known.
notation
620207
Semantic type UMLS property
Has inheritance type
cui
C5703066
OMIM Entry Type
3
OMIM MimType Value
pound
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