NTRK2

neurotrophic receptor tyrosine kinase 2
OMIM: 600456, ClinGen, DECIPHER

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green NTRK2 in Mendeliome Version 1.2302	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Epileptic encephalopathy, early infantile, 58, MIM# 617830 Obesity, hyperphagia, and developmental delay, MIM# 613886
Green NTRK2 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.108 Component of the following Super Panels: Progressive Neurological Conditions	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Epileptic encephalopathy, early infantile, 58, MIM# 617830
Green NTRK2 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.63	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Obesity, hyperphagia, and developmental delay, MIM# 613886
Red NTRK2 in Fetal anomalies Version 1.313	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Genomics England PanelApp Expert list Phenotypes Obesity, hyperphagia, and developmental delay, MIM# 613886 Developmental and epileptic encephalopathy 58, MIM# 617830
Green NTRK2 in Severe early-onset obesity Level 2: Endocrine disorders Version 1.13	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genomics England PanelApp Phenotypes Obesity, hyperphagia, and developmental delay, OMIM:613886