Disease #03648 (ARCL1B (cutis laxa, autosomal recessive, type 1B (ARCL-1B)), OMIM:614437)
Official abbreviation |
ARCL1B |
Name |
cutis laxa, autosomal recessive, type 1B (ARCL-1B) |
OMIM ID |
614437 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
EFEMP2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|