Pascual-Castroviejo syndrome type 1
Timothy syndrome
Noonan syndrome
Treacher Collins syndrome
Weill-Marchesani syndrome
Miller syndrome
Baller-Gerold syndrome
Camurati-Engelmann disease
nevoid basal-cell carcinoma syndrome
Carpenter syndrome
RIDDLE syndrome
ablepharon macrostomia syndrome
incontinentia pigmenti
Axenfeld syndrome
Lowe syndrome
Moebius syndrome
CHARGE syndrome
Pashayan syndrome
Dubowitz syndrome
adermatoglyphia
subsyndrome
Pfeiffer syndrome
pseudolesion
Aarskog-Scott syndrome
Goldenhar syndrome
Feingold syndrome
Cornelia de Lange syndrome
trichothiodystrophy
Williams syndrome
Costello syndrome
abnormality
pathomorphology
abnormalcy
Michelin tire baby syndrome
genetic disorder
piebaldism
idiocrasy
progeria
Waardenburg syndrome
Weaver syndrome
achondrogenesis
ichthyosis bullosa of Siemens
Berk-Tabatznik syndrome
cluster B personality disorder
Rubinstein-Taybi syndrome
Bart syndrome
Levy-Hollister syndrome
aboulomania
hereditary hemorrhagic telangiectasia
depressive personality disorder
Munchausen's syndrome
leontiasis
pathoanatomic
mammalian meat allergy
triple A syndrome
hard-featured
aetiopathogenesis
anodontia
rosacea
FLK
headmate
Munchausen syndrome
Donohue syndrome
defectological
dysostosis multiplex
endotype
mongolianism
mongolism
gargoylism
lipochondrodystrophy
FG syndrome
Down's syndrome
Down syndrome
Hurler's syndrome
Hurler's disease
Marshall syndrome
trisomy 21
prosopamnesia
cardioauditory
acquired disorder
freak
Wolf-Hirschhorn syndrome
autosomal recessive disease
cardiofacial
Lambert-Eaton myasthenic syndrome
oncome
syndromal
autism spectrum disorder
malformation
autosomal recessive defect
Urbach-Wiethe disease
ichthyosis hystrix
clinotype
off the hinges
pathotypic
seropathotype
hypomorphism
syndromically
variation
Fanconi anemia

English words for 'A rare autosomal-recessive condition characterized by facial dysmorphism, cognitive impairment, and skeletal anomalies.'

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