Disease #00127 (SSKS (stiff skin syndrome (SSKS)), OMIM:184900)

Official abbreviation SSKS
Name stiff skin syndrome (SSKS)
OMIM ID 184900
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 0
Associated with 1 gene FBN1
Associated tissues -
Disease features -
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Individuals

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00001221 - - performed exome/genome analysis, detected possibly causative variants but have not yet sufficient evidence to publish - please contact me F no ? (unknown) - - 1 - - SSKS - - - 0 1 Gijs Santen
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