MeSH D000015 - multiple abnormalities
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D000015:
Multiple abnormalities
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D000072661:Ciliopathies
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D000073839:Trisomy 13 syndrome
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D000073842:Trisomy 18 syndrome
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D001478:Basal cell nevus syndrome
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D001506:Beckwith-wiedemann syndrome
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D001816:Bloom syndrome
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D003057:Cockayne syndrome
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D003410:Cri-du-chat syndrome
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D003635:De lange syndrome
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D004314:Down syndrome
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D004476:Ectodermal dysplasia
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D005736:Gardner syndrome
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D007184:Incontinentia pigmenti
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D007690:Polycystic kidney diseases
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D007849:Laurence-moon syndrome
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D008382:Marfan syndrome
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D009261:Nail-patella syndrome
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D009800:Oculocerebrorenal syndrome
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D009958:Orofaciodigital syndromes
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D011218:Prader-willi syndrome
D011535:Prune belly syndrome
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D012410:Congenital rubella syndrome
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D012415:Rubinstein-taybi syndrome
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D012779:Short rib-polydactyly syndrome
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D014849:Waardenburg syndrome
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D015211:Zellweger syndrome
D016142:Holoprosencephaly
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D016715:Proteus syndrome
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D016878:Poems syndrome
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D017204:Angelman syndrome
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D019082:Smith-lemli-opitz syndrome
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D019280:Branchio-oto-renal syndrome
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D020331:Mobius syndrome
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D044542:Leopard syndrome
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D054000:Sebaceous of jadassohn nevus
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D054062:Deaf-blind disorders
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D054463:Trichothiodystrophy syndromes
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D054877:Wolf-hirschhorn syndrome
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D054975:Pallister-hall syndrome
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D055947:Loeys-dietz syndrome
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D056685:Costello syndrome
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D056730:Silver-russell syndrome
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D056731:Donohue syndrome
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D056732:Prolidase deficiency
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D056733:Carney complex
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D056734:Monilethrix
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D056770:Netherton syndrome
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D056830:Isolated noncompaction of the ventricular myocardium
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D056846:Weill-marchesani syndrome
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D056889:Barth syndrome
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D058165:22q11 deletion syndrome
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D058495:Sotos syndrome
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D058496:Smith-magenis syndrome
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D058497:Fraser syndrome
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D058502:Pentalogy of cantrell
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D059446:Heterotaxy syndrome
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