Disease #02779 (IPS (ichthyosis prematurity syndrome (IPS)), OMIM:608649)
| Official abbreviation |
IPS |
| Name |
ichthyosis prematurity syndrome (IPS) |
| OMIM ID |
608649 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
SLC27A4 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2018-11-16 12:05:26 +01:00 (CET) |
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