MYH10

myosin heavy chain 10
OMIM: 160776, Gene2Phenotype

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Amber MYH10 in Anophthalmia_Microphthalmia_Coloboma Level 2: Ophthalmological disorders Version 1.46	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Literature Phenotypes Neurodevelopmental disorder, MONDO:0700092, MYH10-related
Green MYH10 in Mendeliome Version 1.2656	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Expert list Phenotypes AD complex neurodevelopmental disorder with or without congenital anomalies (MONDO:0100465)
Green MYH10 in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.316	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Expert list Phenotypes AD complex neurodevelopmental disorder with or without congenital anomalies (MONDO:0100465)
Green MYH10 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.174	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Expert list Phenotypes AD complex neurodevelopmental disorder with or without congenital anomalies (MONDO:0100465)
Green MYH10 in Fetal anomalies Version 1.370	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Expert list Genomics England PanelApp Phenotypes AD complex neurodevelopmental disorder with or without congenital anomalies (MONDO:0100465)