ischium hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size, usually due to a reduced number of cells, of the lowest of the three major bones that constitute each half of the pelvis, distinct at birth but later becoming fused with the ilium and pubis (Mammalian Phenotype Ontology, MP_0004690)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004690
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Genes

1 gene mutations causing the ischium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
RUNX2 runt-related transcription factor 2