Disease #05286 (LCCS11 (contraction, lethal, congenital syndrome, type 11 (LCCS-11)), OMIM:617194)
| Official abbreviation |
LCCS11 |
| Name |
contraction, lethal, congenital syndrome, type 11 (LCCS-11) |
| OMIM ID |
617194 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
7 |
| Phenotype entries for this disease |
7 |
| Associated with 1 gene |
GLDN |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2017-06-21 13:42:01 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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