Disease #01733 (ARCL-3A (cutis laxa, autosomal recessive, type IIIA (ARCL-3A, De Barsy syndrome)), OMIM:219150)
| Official abbreviation |
ARCL-3A |
| Name |
cutis laxa, autosomal recessive, type IIIA (ARCL-3A, De Barsy syndrome) |
| OMIM ID |
219150 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ALDH18A1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
