MTSS1L

MTSS1L, I-BAR domain containing
OMIM: 616951, ClinGen, DECIPHER

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green MTSS1L in Mendeliome Version 1.2302	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Intellectual developmental disorder with ocular anomalies and distinctive facial features MIM#620086
Green MTSS1L in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.295	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Intellectual developmental disorder with ocular anomalies and distinctive facial features MIM#620086
Amber MTSS1L in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 1.210	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Literature Phenotypes Intellectual developmental disorder with ocular anomalies and distinctive facial features MIM#620086
Green MTSS1L 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 Literature Phenotypes Intellectual developmental disorder with ocular anomalies and distinctive facial features MIM#620086
Green MTSS1L in Congenital nystagmus Level 2: Ophthalmological disorders Version 1.22	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Intellectual developmental disorder with ocular anomalies and distinctive facial features MIM#620086