Alagille syndrome
Birt-Hogg-Dubé syndrome
adermatoglyphia
nephronophthisis
pathogenetics
xanthinuria
genopathy
hereditary hemorrhagic telangiectasia
ablepharon macrostomia syndrome
homocystinuria
hyperbilirubinemia of the newborn
neonatal hyperbilirubinemia
nephropathy
kidney disease
Pallister-Hall syndrome
Prader-Willi syndrome
nephrosis
renal disorder
alkaptonuria
POEMS syndrome
Meckel-Gruber syndrome
alcaptonuria
carnosinemia
genetic disease
inherited disease
hepatosis
genetic disorder
pathoprogression
hereditary condition
inherited disorder
congenital disease
genetic defect
genetic abnormality
hereditary disease
nephrotic syndrome
organic disorder
knock knee
hepatopathy
Zellweger syndrome
liver disease
pachydermoperiostosis
chronic renal failure
cardiogenetics
hepatopathogenesis
chronic kidney failure
McKusick-Kaufman syndrome
polyposis
nevoid basal-cell carcinoma syndrome
Edwards syndrome
Cornelia de Lange syndrome
inborn error of metabolism
dyshepatia
idiopathy
methylmalonic acidemia
Wolf-Hirschhorn syndrome
idiopathic disease
enzymopathy
hyperpipecolatemia
Lesch-Nyhan syndrome
idiopathic disorder
hepatopathology
Sotos syndrome
Cowden syndrome
cystoprotein
Nijmegen breakage syndrome
diseasome
cri du chat syndrome
histidinemia
minimal change disease
natural history
pathophenotype
tyrosinemia
polypathy
hypomorph
hypereosinophily
mutagenesis
interneuronopathy
biliousness
ketoacidemia
purple urine bag syndrome
epidemic
cirrhosis
Hurler's syndrome
Hurler's disease
gargoylism
lipochondrodystrophy
dysostosis multiplex
syndrome X