Amish lethal microcephaly Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Amish lethal microcephaly is a very rare syndrome characterized by extreme microcephaly and early death, within the first year. (Orphanet Rare Disease Ontology, Orphanet_99742)
External Link http://www.omim.org/entry/607196
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Genes

1 genes associated with the Amish lethal microcephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
SLC25A19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19