Birt-Hogg-Dubé syndrome
Meckel-Gruber syndrome
Alagille syndrome
adermatoglyphia
POEMS syndrome
pathogenetics
nephronophthisis
cystic fibrosis transport regulator
CFTR
Cowden syndrome
ablepharon macrostomia syndrome
mucolipin
PKD
polycystic kidney disease
cystoprotein
angiomyolipoma
genetic disorder
beclin
antioncogene
obligate carrier
hereditary hemorrhagic telangiectasia
albuminurophobia
xanthinuria
oncogene
McKusick-Kaufman syndrome
genopathy
nephrocarcinoma
autosomal dominant disease
autosomal recessive defect
autosomal recessive disease
polycystin
autosomal dominant disorder
nephrosis
kidney disease
renal disorder
cancroid
nephropathy
noncancer
pyogranuloma
Joubert syndrome
suicide gene
proto-oncogene
bladder cancer
nephroblastoma
Beckwith-Wiedemann syndrome
primary myelofibrosis
macromutation
chromoplexy
Camurati-Engelmann disease
heteroallele
progeria
hyperpipecolatemia
enzymopathy
Fanconi's anemia
pancreatic fibrosis
CF
oncomutation
Fanconi's anaemia
cystic fibrosis
mutagenesis
mucoviscidosis
congenital pancytopenia
fibrocystic disease of the pancreas
Bloom's syndrome
morphogene
clusterin
nephrosphere
cancerome
morphopathy
tuberous sclerosis
testiculopathy
fibrocarcinoma
candidate
endophenotype
autogynephile
pseudocirrhosis
proposita
previvor
oncogenotype
primary immunodeficiency
polygenic disorder
nephroma
polygenic disease
mutagen