FAMILIAL CIRRHOSIS OF THE   LIVER, RENAL TUBULAR DEFECTS WITH RICKETS AND IMPAIRED TYROSINE METABOLISM.
D002648:Child; D012080:Chronic Kidney Disease-Mineral and Bone Disorder; D030342:Genetic Diseases, Inborn; D005823:Genetics; D006801:Humans; D007223:Infant; D007231:Infant, Newborn; D007674:Kidney Diseases; D007684:Kidney Tubules; D008103:Liver Cirrhosis; D008659:Metabolic Diseases; D009401:Nephrosis; D010667:Phenylpyruvic Acids; D011506:Proteins / Q000378:metabolism*; D000608:Renal Aminoacidurias; D012279:Rickets; D013154:Spleen; D014443:Tyrosine; D014807:Vitamin D
D010667:Phenylpyruvic Acids; D011506:Proteins; D014807:Vitamin D; D014443:Tyrosine; C031606:phenylpyruvic acid
AMINOACIDURIA, RENAL; CHILD; GENETICS; INFANT; INFANT, NEWBORN; KIDNEY DISEASES; KIDNEY TUBULES; LIVER CIRRHOSIS, POSTNECROTIC; METABOLIC DISEASES; NEPHROSIS; PHENYLPYRUVIC ACID; PROTEIN METABOLISM; RICKETS, RENAL; SPLEEN; TYROSINE; VITAMIN D