Label
Description
KFPT:PT-WEXM4B9Z CUI has phenotype Abnormal palate morphology
A Knowledge Graph Assertion from Kids First
KFPT:PT-WEXM4B9Z CUI has phenotype Scoliosis, unspecified
KFPT:PT-WEXM4B9Z CUI has phenotype Phenotypic abnormality
KFPT:PT-WEXM4B9Z CUI has phenotype Urogenital Diseases
KFPT:PT-WEXM4B9Z CUI has phenotype Limited extraocular movements
KFPT:PT-WEXM4B9Z CUI has phenotype Lower cranial nerve dysfunction
KFPT:PT-WEXM4B9Z CUI has phenotype Imaging of brain abnormal
KFPT:PT-WEXM4B9Z CUI has phenotype Facial Paresis
KFPT:PT-WEXM4B9Z CUI has phenotype Hearing abnormality
KFPT:PT-WEXM4B9Z CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation