Gene: SAMD9L ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 219285
Gene Symbol: SAMD9L
SAMD9L 		0.110 GeneticVariation disease BEFREE SAMD9L mutations have been reported in a few families with balance problems and nystagmus due to cerebellar atrophy, and may lead to similar hematological disease as seen in SAMD9 mutation carriers, from early childhood to adult years. 29535429 2018
Entrez Id: 219285
Gene Symbol: SAMD9L
SAMD9L 		0.110 Biomarker disease HPO