SEMA7A

Panel	Reviews	Mode of inheritance	Details
Amber SEMA7A in Cholestasis Level 2: Gastroenterological disorders Version 1.0 Component of the following Super Panels: Liverome Superpanel	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Expert list Phenotypes Cholestasis, progressive familial intrahepatic, 11 , MIM# 619874
Amber SEMA7A in Mendeliome Version 1.2302	2 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Decreased bone mineral density Kallmann syndrome Cholestasis, progressive familial intrahepatic, 11 , MIM# 619874

Panel

Reviews

Mode of inheritance

Details

Level 2: Gastroenterological disorders
Version 1.0

Component of the following Super Panels:

Liverome Superpanel

1 review

BIALLELIC, autosomal or pseudoautosomal

Version 1.2302

2 reviews

BOTH monoallelic and biallelic, autosomal or pseudoautosomal

2 panels