SFTPA1

Panel	Reviews	Mode of inheritance	Details
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Amber SFTPA1 in Interstitial Lung Disease Level 2: Respiratory disorders Version 1.0	2 reviews	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Amber Literature Victorian Clinical Genetics Services Phenotypes Idiopathic pulmonary fibrosis Interstitial lung disease 1, MIM# 619611
Green SFTPA1 in Mendeliome Version 1.2302	1 review	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Idiopathic pulmonary fibrosis Interstitial lung disease 1, MIM# 619611
Green SFTPA1 in Pulmonary Fibrosis_Interstitial Lung Disease Level 2: Respiratory disorders Version 0.84	2 reviews	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Idiopathic pulmonary fibrosis Interstitial lung disease 1, MIM# 619611

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