Disease #00565 (PTHSL-2 (Pitt-Hopkins-like syndrome 2 (PTHSL-2)), OMIM:614325)
| Official abbreviation |
PTHSL-2 |
| Name |
Pitt-Hopkins-like syndrome 2 (PTHSL-2) |
| OMIM ID |
614325 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
NRXN1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
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