Disease #03648 (ARCL1B (cutis laxa, autosomal recessive, type 1B (ARCL-1B)), OMIM:614437)

Official abbreviation ARCL1B
Name cutis laxa, autosomal recessive, type 1B (ARCL-1B)
OMIM ID 614437
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene EFEMP2
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

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00080968 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - ARCL1B Cutis laxa, autosomal recessive, type IB (OMIM:614437) EFEMP2 EFEMP2 1 1 Daniel Trujillano
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