Disease #05192 (ECCL (lipomatosis, encephalocraniocutaneous (ECCL)), OMIM:613001)
| Official abbreviation |
ECCL |
| Name |
lipomatosis, encephalocraniocutaneous (ECCL) |
| OMIM ID |
613001 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
FGFR1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2016-10-11 10:00:03 +02:00 (CEST) |
| Date last edited |
N/A |
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