Disease #05872 (SAO (ovalocytosis, South Asian type (SAO)), OMIM:166900)
Official abbreviation |
SAO |
Name |
ovalocytosis, South Asian type (SAO) |
OMIM ID |
166900 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
SLC4A1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2020-11-08 10:47:16 +01:00 (CET) |
Date last edited |
N/A |
Individuals
|
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