Label
Description
KFPT:PT-R9YTRGTD CUI has phenotype Congenital digestive system anomalies
A Knowledge Graph Assertion from Kids First
KFPT:PT-R9YTRGTD CUI has phenotype Hearing abnormality
KFPT:PT-R9YTRGTD CUI has phenotype Congenital anomaly of face
KFPT:PT-R9YTRGTD CUI has phenotype Phenotypic abnormality
KFPT:PT-R9YTRGTD CUI has phenotype Cardiovascular Abnormalities
KFPT:PT-R9YTRGTD CUI has phenotype Lower cranial nerve dysfunction
KFPT:PT-R9YTRGTD CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation
KFPT:PT-R9YTRGTD CUI has phenotype Scoliosis, unspecified
KFPT:PT-R9YTRGTD CUI has phenotype Abnormal palate morphology
KFPT:PT-R9YTRGTD CUI has phenotype Limited extraocular movements