Disease #02051 (MKS7 (Meckel syndrome, type 7 (MKS-7, Dandy-Walker cyst, renal-hepatic-pancreatic dysplasia)), OMIM:267010)
| Official abbreviation |
MKS7 |
| Name |
Meckel syndrome, type 7 (MKS-7, Dandy-Walker cyst, renal-hepatic-pancreatic dysplasia) |
| OMIM ID |
267010 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
NPHP3 |
| 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) |
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