hereditary hemorrhagic telangiectasia
adermatoglyphia
ablepharon macrostomia syndrome
Timothy syndrome
Camurati-Engelmann disease
organic defect
Noonan syndrome
athrombia
Alagille syndrome
genetic disorder
vasculogenic
dysfibrinogenemia
McKusick-Kaufman syndrome
panvasculopathy
POEMS syndrome
ataxia-telangiectasia
Turner's syndrome
Weaver syndrome
Marfan syndrome
angiosis
Townes-Brocks syndrome
Weill-Marchesani syndrome
Pallister-Hall syndrome
osteopetrosis
pathogenetics
genecologic
Treacher Collins syndrome
Carpenter syndrome
genecological
variation
Feingold syndrome
hemopathy
Lowe syndrome
achondroplasia
monosomy
Marfan's syndrome
xanthinuria
hereditary condition
lipochondrodystrophy
dysostosis multiplex
genecologically
hereditary disease
genetic abnormality
genopathy
Hurler's syndrome
Hurler's disease
genetic disease
angiopathy
genetic defect
inherited disease
gargoylism
congenital disease
Pascual-Castroviejo syndrome type 1
inherited disorder
Wolf-Hirschhorn syndrome
proposita
Nijmegen breakage syndrome
myotonic dystrophy
autosomal dominant disorder
autosomal dominant disease
hyperpipecolatemia
Aicardi syndrome
piebaldism
vasculopathy
pachydermoperiostosis
pathoangiogenesis
congenital contractural arachnodactyly
Birt-Hogg-Dubé syndrome
genetic
Pfeiffer syndrome
ectodermosis
pycnodysostosis
blood disease
blood disorder
Edwards syndrome
Down syndrome
hypervascular
hereditary elliptocytosis
endophenotype
diathesis
congenital heart defect
Cowden syndrome
mutable
chromoanasynthesis
multiomics
propositus
Meckel-Gruber syndrome
cartilage-hair hypoplasia
hemopathology
malformation
hereditarily
monogenic disease
onychogryphotic
angiopathology
monogenic disorder
pathognomic
Bart syndrome
autogynephile
angioproliferation