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genetic disorder
Used for:
Alstrom syndrome
Used for:
Bardet Biedel syndrome
Used for:
Clouston's syndrome
Used for:
corneal dystrophy
Used for:
familial Mediterranean fever
Used for:
hereditary cerebellar degeneration
Used for:
hereditary disorder
Used for:
Joubert syndrome
Used for:
Laurence Moon Biedl syndrome
Used for:
Leigh disease
Used for:
LEOPARD syndrome
Used for:
Multiple Lentigines
Used for:
Rabson Mendenhall syndrome
Used for:
subacute necrotizing encephalomyelopathy
See for:
deformity
See for:
familial disorder
See for:
malformation
Broader Terms:
disease /disorder
Narrower Terms:
achondroplasia
Narrower Terms:
acrodermatitis enteropathica
Narrower Terms:
adrenoleukodystrophy
Narrower Terms:
afibrinogenemia
Narrower Terms:
Alagille syndrome
Narrower Terms:
Alport syndrome
Narrower Terms:
ataxia telangiectasia
Narrower Terms:
cerebrohepatorenal syndrome
Narrower Terms:
chromosome disorder
Narrower Terms:
congenital erythropoietic porphyria
Narrower Terms:
congenital ichthyosis
Narrower Terms:
craniofacial dysostosis
Narrower Terms:
cutis laxa
Narrower Terms:
Ehlers Danlos syndrome
Narrower Terms:
epidermolysis bullosa
Narrower Terms:
familial dysautonomia
Narrower Terms:
familial hypothyroidism
Narrower Terms:
Friedreich's ataxia
Narrower Terms:
Fuchs' dystrophy
Narrower Terms:
happy puppet syndrome
Narrower Terms:
hemoglobinopathy
Narrower Terms:
hemophilia A
Narrower Terms:
hemophilia B
Narrower Terms:
hereditary elliptocytosis
Narrower Terms:
hereditary peripheral nervous system disorder
Narrower Terms:
hereditary spherocytosis
Narrower Terms:
Holt Oram syndrome
Narrower Terms:
Huntington's disease
Narrower Terms:
hypoprothrombinemia
Narrower Terms:
inborn metabolism disorder
Narrower Terms:
keratosis follicularis
Narrower Terms:
Li Fraumeni syndrome
Narrower Terms:
Marfan syndrome
Narrower Terms:
multiple endocrine neoplasia
Narrower Terms:
muscular dystrophy
Narrower Terms:
myotonia congenita
Narrower Terms:
neurofibromatosis
Narrower Terms:
osteogenesis imperfecta
Narrower Terms:
polycystic kidney
Narrower Terms:
protoporphyria
Narrower Terms:
pseudoxanthoma elasticum
Narrower Terms:
retinitis pigmentosa
Narrower Terms:
retinoblastoma
Narrower Terms:
Rett syndrome
Narrower Terms:
testicular feminization
Narrower Terms:
tuberous sclerosis
Narrower Terms:
Usher syndrome
Narrower Terms:
Von Hippel Lindau syndrome
Narrower Terms:
von Willebrand's disease
Narrower Terms:
Waardenburg syndrome
Narrower Terms:
Werner's syndrome
Narrower Terms:
Wilms' tumor
Narrower Terms:
Wiskott Aldrich syndrome
Narrower Terms:
xeroderma pigmentosum
Related Terms:
acanthosis nigricans
Related Terms:
color blindness
Related Terms:
congenital aplastic anemia
Related Terms:
congenital blood disorder
Related Terms:
congenital disorder
Related Terms:
dyserythropoietic anemia
Related Terms:
family genetics
Related Terms:
genetic susceptibility
Related Terms:
hypertrophic osteoarthropathy
Related Terms:
malignant hyperthermia
Related Terms:
obesity
Related Terms:
psoriasis
Scope Note:
general term for any disorder caused by a genetic mechanism, comprising chromosome aberrations or anomalies, mendelian or monogenic or single-gene disorders, and multifactorial disorders; note that all genetic disorders are not treed under this term; see RTs for others; in addition, many disorders not treed here or under RTs may have a genetic component.
Term Number:
1254-7727
Send your comments to: Melody Lowe