Disease #04623 (HJS2;MRD36 (Houge-Janssens syndrome, type 2), OMIM:616362)
| Official abbreviation |
HJS2;MRD36 |
| Name |
Houge-Janssens syndrome, type 2 |
| OMIM ID |
616362 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
PPP2R1A |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:23 +02:00 (CEST) |
| Date last edited |
2025-03-18 19:44:50 +01:00 (CET) |
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