Disease #05708 (FHCL1 (hypercholesterolemia, familial, type 1 (FHCL1)), OMIM:143890)

Official abbreviation FHCL1
Name hypercholesterolemia, familial, type 1 (FHCL1)
OMIM ID 143890
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 4 genes APOA2, EPHX2, GHR, LDLR
Associated tissues -
Disease features -
Remarks -
Date created 2020-02-26 12:52:07 +01:00 (CET)
Date last edited N/A


Individuals

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00451601 3bINP-058 PubMed: Vela-Amieva 2024 Familial case (mother affected) M no Mexico Mexican - - - - FHCL1 Bilateral cryptorchidism LDLR LDLR 1 1 Miriam Erandi Reyna-Fabián
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