Disease #04545 (MKS12 (Meckel syndrome?, type 12 (MKS-12)), OMIM:616258)
| Official abbreviation |
MKS12 |
| Name |
Meckel syndrome?, type 12 (MKS-12) |
| OMIM ID |
616258 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
5 |
| Phenotype entries for this disease |
5 |
| Associated with 1 gene |
KIF14 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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