Disease #00086 (GPHYSD2 (GELEOPHYSIC DYSPLASIA 2), OMIM:614185)

Official abbreviation GPHYSD2
Name GELEOPHYSIC DYSPLASIA 2
OMIM ID 614185
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene FBN1
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-16 09:13:52 +00:00 (UTC)
Date last edited N/A

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