Disease #05071 (LCCS6 (contracture syndrome?, lethal, congenital, type 6 (LCCS-6)), OMIM:616248)
| Official abbreviation |
LCCS6 |
| Name |
contracture syndrome?, lethal, congenital, type 6 (LCCS-6) |
| OMIM ID |
616248 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ZBTB42 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 11:00:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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