Phenotypes for disease #01734 (ARCL2A (cutis laxa, autosomal recessive, type IIA (ARCL-2A)), OMIM:219200)

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AscendingPhenotype ID     

Phenotype details     

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Individual ID     
0000223050 generalized skin wrinkling, delayed closure of the anterior fontanelle. Cutis Laxa ARCL2A Familial, autosomal recessive 25y 24y - - - Carmela Fusco 00289442
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