Preferred Name |
Elliptocytosis, Hereditary [Disease/Finding] |
|
Synonyms |
Elliptocytosis, Hereditary |
|
ID |
http://purl.bioontology.org/ontology/NDFRT/N0000001064 |
|
altLabel |
Elliptocytosis, Hereditary Ovalocytosis, Hereditary |
|
cui |
C0013902 |
|
MESH DEFINITION |
An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape. |
|
MESH DUI |
D004612 |
|
MeSH name |
Elliptocytosis, Hereditary |
|
MESH UI |
M0007240 |
|
NDFRT kind |
DISEASE_KIND |
|
notation |
N0000001064 |
|
NUI |
N0000001064 |
|
prefLabel |
Elliptocytosis, Hereditary [Disease/Finding] |
|
SNOMED CID |
191169008 178935009 |
|
tui |
T047 |
|
subClassOf |
Create mapping