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Summary Literature (0)
MIM:613177 - CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C

Xenbase Genes: ltbp4

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013170 - cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies

Disease Ontology (DO):
DOID:0070139 - autosomal recessive cutis laxa type IC
DOID:3144 - cutis laxa