DCC

DCC netrin 1 receptor
OMIM: 120470, Gene2Phenotype

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Red DCC in Cerebral Palsy Level 2: Neurology and neurodevelopmental disorders Version 1.356	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Phenotypes Mirror movements 1 and/or agenesis of the corpus callosum, MIM#157600
Green DCC in Mendeliome Version 1.1902	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Victorian Clinical Genetics Services Phenotypes Mirror movements 1 and/or agenesis of the corpus callosum, OMIM #157600 Gaze palsy, familial horizontal, with progressive scoliosis, 2,OMIM # 617542
Green DCC in Callosome Level 2: Neurology and neurodevelopmental disorders Version 0.522	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Agenesis of the corpus callosum
Green DCC in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.285	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Literature NHS GMS Victorian Clinical Genetics Services Phenotypes Gaze palsy, familial horizontal, with progressive scoliosis, 2, MIM# 617542
Green DCC in Mirror movements Level 2: Neurology and neurodevelopmental disorders Version 1.0	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Mirror movements 1 and/or agenesis of the corpus callosum MIM#157600
Green DCC in Fetal anomalies Version 1.255	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Phenotypes Mirror movements 1 and/or agenesis of the corpus callosum, OMIM #157600 Gaze palsy, familial horizontal, with progressive scoliosis, 2,OMIM # 617542