Phenotypes for disease #01732 (ARCL1A (cutis laxa, autosomal recessive, type IA (ARCL-1A)), OMIM:219100)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000061059 generalized congenital cutis laxa with facial involvement, severe emphysema, inguinal hernias, peripheral pulmonary artery stenosis, pyloric stenosis, mild aortic and tricuspid valve regurgitation - - Familial, autosomal recessive 11m - 0m - - Bert Callewaert 00081474
0000061060 congenital cutis laxa (with facial involvement), severe emphysema, normal cardiac status on echocardiography, high broad forehead, low broad nasal bridge, beaked nose, larage dysplastic ears, sagging cheeks, everted lower lip, photophobia, normal mental status, hypotonia - - Familial, autosomal recessive 1y7m - 0m - - Bert Callewaert 00081475
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