Disease #04532 (SCN6 (neutropenia, severe congenital, type 6, autosomal recessive (SCN-6)), OMIM:616022)
| Official abbreviation |
SCN6 |
| Name |
neutropenia, severe congenital, type 6, autosomal recessive (SCN-6) |
| OMIM ID |
616022 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
JAGN1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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