Disease #00114 (HCS (Holocarboxylase Synthetase Deficiency), OMIM:253270)
Official abbreviation |
HCS |
Name |
Holocarboxylase Synthetase Deficiency |
OMIM ID |
253270 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 0 genes |
- |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-04-22 11:56:16 +08:00 (CST) |
Date last edited |
2021-10-17 16:39:23 +08:00 (CST) |
Individuals
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