Label
Description
KFPT:PT-V3BZMA7X CUI has phenotype Arnold Chiari Malformation
A Knowledge Graph Assertion from Kids First
KFPT:PT-V3BZMA7X CUI has phenotype Congenital blindness
KFPT:PT-V3BZMA7X CUI has phenotype Syndactyly of fingers
KFPT:PT-V3BZMA7X CUI has phenotype Retinal vascular tortuosity
KFPT:PT-V3BZMA7X CUI has phenotype Port-Wine Stain
KFPT:PT-V3BZMA7X CUI has phenotype Subglottic stenosis
KFPT:PT-V3BZMA7X CUI has phenotype Tetralogy of Fallot
KFPT:PT-V3BZMA7X CUI has phenotype Sandal gap
KFPT:PT-V3BZMA7X CUI has phenotype Polycystic Kidney - body part
KFPT:PT-V3BZMA7X CUI has phenotype Wide spaced nipples