Disease #00152 (LDS3 (LOEYS-DIETZ SYNDROME 3), OMIM:613795)
Official abbreviation |
LDS3 |
Name |
LOEYS-DIETZ SYNDROME 3 |
OMIM ID |
613795 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
SMAD3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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