Label
Description
KFPT:PT-7MQFGW6D CUI has phenotype Congenital malrotation of intestine
A Knowledge Graph Assertion from Kids First
KFPT:PT-7MQFGW6D CUI has phenotype Craniosynostosis
KFPT:PT-7MQFGW6D CUI has phenotype Branchioma
KFPT:PT-7MQFGW6D CUI has phenotype Spinal fusion
KFPT:PT-7MQFGW6D CUI has phenotype Pyloric Stenosis, Hypertrophic
KFPT:PT-7MQFGW6D CUI has phenotype Asplenia Syndrome
KFPT:PT-7MQFGW6D CUI has phenotype Congenital blindness
KFPT:PT-7MQFGW6D CUI has phenotype Gastroesophageal reflux disease
KFPT:PT-7MQFGW6D CUI has phenotype Micropenis
KFPT:PT-7MQFGW6D CUI has phenotype Tetralogy of Fallot