Phenotype: abnormal physiological umbilical hernia morphology

Definition
any structural anomaly in the developmental umbilical hernia that occurs when the elongating intestine herniates into the base of the umbilical cord, this normally resolves when the size of the abdomen increases
0%
of tested genes
0
significant genes
0
tested genes

IMPC Gene variants with abnormal physiological umbilical hernia morphology

Phenotype associations to genes and alleles will be available once data has completed quality control.

 The way we measure

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