KFPT:PT-GTMPVXC9 CUI (Kfpt)

KFPT:PT-GTMPVXC9 CUI has phenotype Imaging of brain abnormal

KFPT:PT-GTMPVXC9 CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation

KFPT:PT-GTMPVXC9 CUI has phenotype Congenital digestive system anomalies

KFPT:PT-GTMPVXC9 CUI has phenotype Limited extraocular movements

KFPT:PT-GTMPVXC9 CUI has phenotype Abnormal palate morphology

KFPT:PT-GTMPVXC9 CUI has phenotype Hearing abnormality

KFPT:PT-GTMPVXC9 CUI has phenotype Phenotypic abnormality

KFPT:PT-GTMPVXC9 CUI has phenotype Urogenital Diseases

KFPT:PT-GTMPVXC9 CUI has phenotype Facial Paresis

KFPT:PT-GTMPVXC9 CUI has phenotype Lower cranial nerve dysfunction