deficiency (Surfactant metabolism dysfunction, pulmonary, 3) CPT deficiency, hepatic, type II Cutis laxa, Autosomal Recessive, type IIA Cystic fibrosis Cystinosis,CTNS-related
[zerlaboratories.com]
[…] type IId Congenital disorder of glycosylation, type Im Congenital disorder of glycosylation, type It Congenital myopathy Congenital recessive ichthyoses (CRI) Congenital surfactant
[zerlaboratories.com]