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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