Disease #02687 (SFWHS (skin fragility, woolly hair syndrome (SFWHS)), OMIM:607655)
| Official abbreviation |
SFWHS |
| Name |
skin fragility, woolly hair syndrome (SFWHS) |
| OMIM ID |
607655 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
DSP |
| Associated tissues |
- |
| Disease features |
autosomal recessive |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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