Disease #00089 (SSKS (STIFF SKIN SYNDROME), OMIM:184900)

Official abbreviation SSKS
Name STIFF SKIN SYNDROME
OMIM ID 184900
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
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 09:15:27 +00:00 (UTC)
Date last edited N/A

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