Disease #04512 (GRDF (growth restriction, severe, with distinctive facies (GRDF)), OMIM:616489)

Official abbreviation GRDF
Name growth restriction, severe, with distinctive facies (GRDF)
OMIM ID 616489
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene IGF2
Associated tissues -
Disease features -
Remarks -