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 1.50	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Literature Phenotypes Neurodevelopmental disorder, MONDO:0700092, MYH10-related
Green MYH10 in Mendeliome Version 1.3512	1 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 1.357	1 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 1.410	1 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 1.465	2 reviews	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)