Käsitteen tiedot
Käytettävä termi
Abnormalities, Multiple
Tyyppi
-
Topical Descriptor
Yläkäsite
Alakäsitteet
- 22q11 Deletion Syndrome
- Alagille Syndrome
- Angelman Syndrome
- Barth Syndrome
- Basal Cell Nevus Syndrome
- Beckwith-Wiedemann Syndrome
- Bloom Syndrome
- Branchio-Oto-Renal Syndrome
- Carney Complex
- CHARGE Syndrome
- Ciliopathies
- Cockayne Syndrome
- Costello Syndrome
- Cri-du-Chat Syndrome
- Deaf-Blind Disorders
- De Lange Syndrome
- Donohue Syndrome
- Down Syndrome
- Ectodermal Dysplasia
- Fraser Syndrome
- Gardner Syndrome
- Heterotaxy Syndrome
- Holoprosencephaly
- Incontinentia Pigmenti
- Isolated Noncompaction of the Ventricular Myocardium
- Laurence-Moon Syndrome
- LEOPARD Syndrome
- Loeys-Dietz Syndrome
- Marfan Syndrome
- Mobius Syndrome
- Monilethrix
- Nail-Patella Syndrome
- Netherton Syndrome
- Oculocerebrorenal Syndrome
- Orofaciodigital Syndromes
- Pallister-Hall Syndrome
- Pentalogy of Cantrell
- POEMS Syndrome
- Prader-Willi Syndrome
- Prolidase Deficiency
- Proteus Syndrome
- Prune Belly Syndrome
- Rubella Syndrome, Congenital
- Rubinstein-Taybi Syndrome
- Short Rib-Polydactyly Syndrome
- Silver-Russell Syndrome
- Smith-Lemli-Opitz Syndrome
- Smith-Magenis Syndrome
- Sotos Syndrome
- Trichothiodystrophy Syndromes
- Trisomy 13 Syndrome
- Trisomy 18 Syndrome
- Waardenburg Syndrome
- Weill-Marchesani Syndrome
- Wolf-Hirschhorn Syndrome
- Zellweger Syndrome
Ohjaustermit
- Multiple Abnormalities
Huomautus
- coordinate with specific abnormalities
Käyttöhuomautus
- Congenital abnormalities that affect more than one organ or body structure.
Huomautus muutoshistoriasta
- 68
Muunkieliset termit
-
ruotsi
-
suomi
-
monideformiteetit
-
monimalformaatiot
-
multippelit deformiteetit
-
multippelit epämuodostumat
-
multippelit malformaatiot
URI
http://www.yso.fi/onto/mesh/D000015
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