TBC1D7

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green TBC1D7 in Macrocephaly_Megalencephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 0.149	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Macrocephaly/megalencephaly syndrome, autosomal recessive, MIM# 248000
Green TBC1D7 in Mendeliome Version 1.2302	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Macrocephaly/megalencephaly syndrome, autosomal recessive, MIM# 248000
Red TBC1D7 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.108 Component of the following Super Panels: Progressive Neurological Conditions	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Macrocephaly/megalencephaly syndrome, autosomal recessive MIM#248000
Green TBC1D7 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.63	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genetic Health Queensland Phenotypes Macrocephaly/megalencephaly syndrome, autosomal recessive, MIM# 248000
Amber TBC1D7 in Fetal anomalies Version 1.313	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Macrocephaly/megalencephaly syndrome, autosomal recessive - MIM#248000

5 panels