Disease #00192 (ARCI2 (ichthyosis, congenital, autosomal recessive, type 2 (ARCI-2)), OMIM:242100)

Official abbreviation ARCI2
Name ichthyosis, congenital, autosomal recessive, type 2 (ARCI-2)
OMIM ID 242100
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 2 genes ALOX12B, TGM1
Associated tissues -
Disease features -
Remarks -
Date created 2013-09-08 18:23:51 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00002516 - PubMed: Raghunath 2003 LI Family, Patients V.S. and N.S., self-healing collodion babies F no Yugoslavia Albanian - - - - ARCI2 collodion, self-healing TGM1 TGM1 1 1 Michel van Geel
00003232 - PubMed: Raghunath 2003 LI Family, patients V.S. and N.S., self-healing collodion babies F no Yugoslavia Albanian - - - - ARCI2 collodion, self-healing TGM1 TGM1 1 1 Michel van Geel
00305942 41 - - M - China - - - - - ARCI2 - ALOX12B ALOX12B 2 1 Sha Hong
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