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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