Mesh term Abnormalities, Multiple
Browse to parent terms:Congenital Abnormalities
Description
Congenital abnormalities that affect more than one organ or body structure.Browse to child terms:
22q11 Deletion Syndrome
Alagille Syndrome
Angelman Syndrome
Barth Syndrome
Basal Cell Nevus Syndrome
Beckwith-Wiedemann Syndrome
Bloom Syndrome
Branchio-Oto-Renal Syndrome
CHARGE Syndrome
Carney Complex
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
LEOPARD Syndrome
Laurence-Moon Syndrome
Loeys-Dietz Syndrome
Marfan Syndrome
Mobius Syndrome
Monilethrix
Nail-Patella Syndrome
Netherton Syndrome
Nevus, Sebaceous of Jadassohn
Oculocerebrorenal Syndrome
Orofaciodigital Syndromes
POEMS Syndrome
Pallister-Hall Syndrome
Pentalogy of Cantrell
Polycystic Kidney Diseases
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
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