Disease #00199 (TSC1 (TSC COMPLEX SUBUNIT 1), OMIM:191100)

Official abbreviation TSC1
Name TSC COMPLEX SUBUNIT 1
OMIM ID 191100
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TSC1
Associated tissues -
Disease features -
Remarks -
Date created 2023-10-02 09:34:45 +00:00 (UTC)
Date last edited N/A

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