Label
Description
KFPT:PT-1M4BR97W CUI has phenotype Urogenital Diseases
A Knowledge Graph Assertion from Kids First
KFPT:PT-1M4BR97W CUI has phenotype Hearing abnormality
KFPT:PT-1M4BR97W CUI has phenotype Cardiovascular Abnormalities
KFPT:PT-1M4BR97W CUI has phenotype Congenital anomaly of face
KFPT:PT-1M4BR97W CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation
KFPT:PT-1M4BR97W CUI has phenotype Phenotypic abnormality
KFPT:PT-1M4BR97W CUI has phenotype Imaging of brain abnormal
KFPT:PT-1M4BR97W CUI has phenotype Facial Paresis
KFPT:PT-1M4BR97W CUI has phenotype Limited extraocular movements
KFPT:PT-1M4BR97W CUI has phenotype Congenital digestive system anomalies