Disease #03649 (ARCL3B (cutis laxa, autosomal recessive, type 3B (ARCL-3B)), OMIM:614438)
Official abbreviation |
ARCL3B |
Name |
cutis laxa, autosomal recessive, type 3B (ARCL-3B) |
OMIM ID |
614438 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
PYCR1 |
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
|