Concept information
Término preferido
Abnormalities, Multiple
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Tipo
-
mesh:Descriptor
Definición
- Congenital abnormalities that affect more than one organ or body structure.
Concepto genérico
Conceptos específicos
- 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
- De Lange Syndrome
- Deaf-Blind Disorders
- 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
Etiquetas alternativas
- Multiple Abnormalities
En otras lenguas
-
francés
-
Anomalies congénitales multiples
-
Anomalies multiples congénitales
URI
http://data.loterre.fr/ark:/67375/JVR-W90HVV4Q-T
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