Disease #00685 (LCCS2 (contracture syndrome, lethal, congenital, type 2 (LCCS-2)), OMIM:607598)
Official abbreviation |
LCCS2 |
Name |
contracture syndrome, lethal, congenital, type 2 (LCCS-2) |
OMIM ID |
607598 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
ERBB3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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