KFPT:PT-QR4Q06B1 CUI (Kfpt)

KFPT:PT-QR4Q06B1 CUI has phenotype Lower cranial nerve dysfunction

KFPT:PT-QR4Q06B1 CUI has phenotype Imaging of brain abnormal

KFPT:PT-QR4Q06B1 CUI has phenotype Hearing abnormality

KFPT:PT-QR4Q06B1 CUI has phenotype Abnormal palate morphology

KFPT:PT-QR4Q06B1 CUI has phenotype Facial Paresis

KFPT:PT-QR4Q06B1 CUI has phenotype Scoliosis, unspecified

KFPT:PT-QR4Q06B1 CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation

KFPT:PT-QR4Q06B1 CUI has phenotype Congenital digestive system anomalies

KFPT:PT-QR4Q06B1 CUI has phenotype Cardiovascular Abnormalities

KFPT:PT-QR4Q06B1 CUI has phenotype Urogenital Diseases