TBC1D32

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green TBC1D32 in Ciliopathies Level 2: Dysmorphic and congenital abnormality syndromes Version 1.54	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Orofaciodigital syndrome type IX
Green TBC1D32 in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Orofaciodigital syndrome type IX syndromic hypopituitarism
Red TBC1D32 in Callosome Level 2: Neurology and neurodevelopmental disorders Version 0.522	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Orofaciodigital syndrome type IX
Amber TBC1D32 in Pituitary hormone deficiency Level 2: Endocrine disorders Version 0.34	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Syndromic hypopituitarism
Green TBC1D32 in Fetal anomalies Version 1.255	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Phenotypes Orofacial digital syndrome type IX

5 panels