KDM3B

lysine demethylase 3B
OMIM: 609373, ClinGen, DECIPHER

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Red KDM3B in Cerebral Palsy Level 2: Neurology and neurodevelopmental disorders Version 1.389	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Phenotypes Diets-Jongmans syndrome, MIM#618846
Green KDM3B in Mendeliome Version 1.2302	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Diets-Jongmans syndrome, MIM# 618846 Intellectual disability dysmorphic features short stature
Green KDM3B in Cancer Predisposition_Paediatric Level 2: Cancer Version 0.131	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Diets-Jongmans syndrome, MIM# 618846 Cancer predisposition
Green KDM3B in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 1.210	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Phenotypes Diets-Jongmans syndrome, MIM# 618846 Intellectual disability short stature deafness
Green KDM3B in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.63	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Diets-Jongmans syndrome, MIM# 618846 Intellectual disability dysmorphic features short stature
Green KDM3B in Growth failure Version 1.76	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genomics England PanelApp Phenotypes Diets-Jongmans syndrome, MIM# 618846 Intellectual disability short stature deafness