Label
Description
KFPT:PT-WGG3XRER CUI has phenotype Scoliosis, unspecified
A Knowledge Graph Assertion from Kids First
KFPT:PT-WGG3XRER CUI has phenotype Limited extraocular movements
KFPT:PT-WGG3XRER CUI has phenotype Lower cranial nerve dysfunction
KFPT:PT-WGG3XRER CUI has phenotype Abnormal palate morphology
KFPT:PT-WGG3XRER CUI has phenotype Hearing abnormality
KFPT:PT-WGG3XRER CUI has phenotype Urogenital Diseases
KFPT:PT-WGG3XRER CUI has phenotype Facial Paresis
KFPT:PT-WGG3XRER CUI has phenotype Phenotypic abnormality
KFPT:PT-WGG3XRER CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation
KFPT:PT-WGG3XRER CUI has phenotype Cardiovascular Abnormalities