30 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Fgf23tm1Blan/Fgf23+ PhexHyp/Y Not Specified	abnormal long bone metaphysis morphology	J:94041
	increased diameter of femur	J:94041
	short femur	J:94041
Fgf23tm1Blan/Fgf23tm1Blan PhexHyp/Y Not Specified	abnormal bone mineralization	J:94041
	abnormal femur morphology	J:94041
	decreased diameter of femur	J:94041
	increased circulating phosphate level	J:94041
	long femur	J:94041
Fgf23tm1Blan/Fgf23tm1Blan Sfrp4tm1.1Blan/Sfrp4tm1.1Blan involves: 129 * C57BL/6	abnormal digestive system morphology	J:173962
	calcified artery	J:173962
	decreased body size	J:173962
	emphysema	J:173962
	increased circulating phosphate level	J:173962
	nephrocalcinosis	J:173962
	premature death	J:173962
Fgf23tm1Blan/Fgf23tm1Blan Vdrtm1Rge/Vdrtm1Rge involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6	epidermal cyst	J:121006
	normal homeostasis/metabolism phenotype	J:121006
	increased circulating alkaline phosphatase level	J:121006
	increased circulating parathyroid hormone level	J:121006
Fgf23tm1Sliu/Fgf23+ PhexHyp/Y involves: 129S/SvEv * C57BL/6	abnormal vitamin D level	J:110579
	decreased body weight	J:110579
	decreased circulating phosphate level	J:110579
	increased bone mineral density	J:110579
	long femur	J:110579
	rickets	J:110579
Fgf23tm1Sliu/Fgf23tm1Sliu PhexHyp/Y involves: 129S/SvEv * C57BL/6	abnormal circulating calcium level	J:110579
	abnormal circulating phosphate level	J:110579
	abnormal long bone epiphyseal plate morphology	J:110579
	abnormal postnatal growth/weight/body size	J:110579
	abnormal vitamin D level	J:110579
	decreased body length	J:110579
	decreased body weight	J:110579
	decreased bone mineral density	J:110579
	decreased circulating parathyroid hormone level	J:110579
	premature death	J:110579
	rickets	J:110579
	short femur	J:110579