Fanconi anemia
preleukemia
achondrogenesis
Baller-Gerold syndrome
leukemogenicity
Aarskog-Scott syndrome
Nijmegen breakage syndrome
Larsen syndrome
Pallister-Hall syndrome
Weill-Marchesani syndrome
Waardenburg syndrome
dyskeratosis congenita
Edwards syndrome
genetic disorder
Cornelia de Lange syndrome
ectromelia
leukemogenic
cartilage-hair hypoplasia
abnormality
Costello syndrome
Beckwith-Wiedemann syndrome
ablepharon macrostomia syndrome
faciodigitogenital dysplasia
abnormalcy
Miller syndrome
pseudolesion
CHARGE syndrome
holoprosencephaly
mongolianism
Down syndrome
Marshall syndrome
trisomy 21
mongolism
nail-patella syndrome
Down's syndrome
achondroplasia
incontinentia pigmenti
leukemic
Noonan syndrome
Townes-Brocks syndrome
aniridia
dysmorphology
hypogenesis
Duane syndrome
tetra-amelia
leukaemic
monosomy
acute lymphocytic leukemia
aleukia
acute lymphoblastic leukemia
excrescent
Léri-Weill dyschondrosteosis
acquired disorder
Goldenhar syndrome
Keutel syndrome
malformation
Lowe syndrome
Stickler syndrome
Nager acrofacial dysostosis
abrachiocephalia
metabola
Moebius syndrome
CD135
mutationistic
Shwachman-Diamond syndrome
acephalism
plagiocephaly
Pascual-Castroviejo syndrome type 1
mutate
mutagenize
Bart syndrome
phocomelia
Berk-Tabatznik syndrome
dwarf
homunculus
nanism
abrachiocephaly
CHILD syndrome
Pfeiffer syndrome
mannikin
manikin
ectrodactyly
POEMS syndrome
polymelia
acephalocheiria
macroglossia
erythroleukemia
true dwarf
primordial dwarf
leukemogenically
embryopathy
hypoplastic dwarf
normal dwarf
Langer-Giedion syndrome
Mendes da Costa syndrome

English words for 'A rare genetic disease typically leading to acute myelogenous leukemia, and often accompanied by congenital defects such as short stature, abnormalities of the skin, arms, head, eyes, kidneys, and ears, and developmental disabilities.'

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