Bardet-Biedl syndrome
Laurence-Moon syndrome
gargoylism
dysostosis multiplex
Hurler's syndrome
Hurler's disease
lipochondrodystrophy
Townes-Brocks syndrome
Meckel-Gruber syndrome
nail-patella syndrome
Keutel syndrome
pathogenetics
polycythemic
inborn error of metabolism
Börjeson–Forssman–Lehmann syndrome
Pallister-Hall syndrome
Bart syndrome
homocystinuria
Lowe syndrome
Aicardi syndrome
FG syndrome
Cornelia de Lange syndrome
polychromia
Birt-Hogg-Dubé syndrome
Baller-Gerold syndrome
polyhaemia
Alagille syndrome
xanthinuria
null
Wolf-Hirschhorn syndrome
Urbach-Wiethe disease
Joubert syndrome
pachydermoperiostosis
polychromatophilic
primary immunodeficiency
faciodigitogenital dysplasia
Feingold syndrome
pathomorphology
prionopathy
pelorized
pathomorphosis
polycrotic
cartilage-hair hypoplasia
Miller syndrome
ablepharon macrostomia syndrome
neomorphic
Carpenter syndrome
purple urine bag syndrome
retinoblastoma protein
mucopolysaccharidosis
Brunner syndrome
normophilic
polyemic
morphopathological
metabolic disorder
nephronophthisis
Lesch-Nyhan syndrome
POEMS syndrome
Prader-Willi syndrome
Norrie disease
Marinesco-Sjögren syndrome
Sotos syndrome
hypomorph
polyuric
genopathy
Aicardi-Goutières syndrome
ambiphilicity
GAPO syndrome
Costello syndrome
metachromatic leukodystrophy
Waardenburg syndrome
diseasome
subhealth
amorphic
Edwards syndrome
incontinentia pigmenti
pathological state
morbosity
abnormalcy
amorph
Weill-Marchesani syndrome
Langer-Giedion syndrome
abnormality
nephrotic syndrome
overdiuresis
Wilson's disease
nephrosis
rickettsiemic
Fanconi anemia
prionosis
citrin
pycnodysostosis
plurimetabolic
metabola
polyposis
seipinopathy
Lambert-Eaton myasthenic syndrome
polymitotic
bad
osteopetrosis

English words for 'A ciliopathic human genetic disorder characterized principally by obesity, retinitis pigmentosa, polydactyly, hypogonadism, and renal failure in some cases.'

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