Label
Description
KFPT:PT-VTN6B0QP CUI has phenotype Imaging of brain abnormal
A Knowledge Graph Assertion from Kids First
KFPT:PT-VTN6B0QP CUI has phenotype Urogenital Diseases
KFPT:PT-VTN6B0QP CUI has phenotype Lower cranial nerve dysfunction
KFPT:PT-VTN6B0QP CUI has phenotype Hearing abnormality
KFPT:PT-VTN6B0QP CUI has phenotype Limited extraocular movements
KFPT:PT-VTN6B0QP CUI has phenotype Phenotypic abnormality
KFPT:PT-VTN6B0QP CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation
KFPT:PT-VTN6B0QP CUI has phenotype Cardiovascular Abnormalities
KFPT:PT-VTN6B0QP CUI has phenotype Congenital anomaly of face
KFPT:PT-VTN6B0QP CUI has phenotype Scoliosis, unspecified