MANF

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Amber MANF in Mendeliome Version 1.1891	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Expert Review Phenotypes Diabetes, deafness, developmental delay, and short stature syndrome, MIM# 620651
Amber MANF in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 1.194	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Expert Review Phenotypes Diabetes, deafness, developmental delay, and short stature syndrome, MIM# 620651
Amber MANF in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Expert Review Phenotypes Diabetes, deafness, developmental delay, and short stature syndrome, MIM# 620651
Amber MANF in Monogenic Diabetes Level 2: Endocrine disorders Version 0.134 Component of the following Super Panels: Metabolic Disorders Superpanel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Expert Review Phenotypes Diabetes, deafness, developmental delay, and short stature syndrome, MIM# 620651
Green MANF in Incidentalome_PREGEN_DRAFT Version 0.43	review	Unknown	Sources NSW Health Pathology Expert Review Green

5 panels