Disease #00726 (SCN-4 (neutropenia, severe congenital, type 4, autosomal recessive (SCN-4)), OMIM:612541)
| Official abbreviation |
SCN-4 |
| Name |
neutropenia, severe congenital, type 4, autosomal recessive (SCN-4) |
| OMIM ID |
612541 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
G6PC3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
