Disease #06650 (DMJDS1 (dysplasia, diencephalic-mesencephalic junction, syndrome 1), OMIM:251280)
Official abbreviation |
DMJDS1 |
Name |
dysplasia, diencephalic-mesencephalic junction, syndrome 1 |
OMIM ID |
251280 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
PCDH12 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
N/A |
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