Disease #03808 (ARCI9 (ichthyosis, congenital, autosomal recessive, type 9 (ARCI-9)), OMIM:615023)

Official abbreviation ARCI9
Name ichthyosis, congenital, autosomal recessive, type 9 (ARCI-9)
OMIM ID 615023
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 6
Phenotype entries for this disease 6
Associated with 1 gene CERS3
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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00104974 - - - M yes (Iran) Persian - - - - ARCI9 - CERS3 CERS3 1 2 Hassan Vahidnezhad
00104975 - - - F yes Iran - - - - - ARCI9 - CERS3 CERS3 1 1 Hassan Vahidnezhad
00104976 - - - M yes Iran - - - - - ARCI9 - CERS3 CERS3 1 1 Hassan Vahidnezhad
00104977 - - - M yes Iran - - - - - ARCI9 - CERS3 CERS3 1 1 Hassan Vahidnezhad
00104978 - - - M yes Iran - - - - - ARCI9 - CERS3 - - 1 Hassan Vahidnezhad
00105001 - - - F yes Iran Persian - - - - ARCI9 - CERS3 CERS3 1 1 Hassan Vahidnezhad
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