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Parent Node:
expanddiaphragmatic or abdominal wall malformation (MONDO:0020021)
..Starting node
..expandsyndromic diaphragmatic or abdominal wall malformation ()

       Child Nodes:
........expandcloacal exstrophy (disease) ()
........expandCornelia de Lange syndrome ()
........expandcutis laxa ()
........expanddiaphragmatic defect-limb deficiency-skull defect syndrome ()
........expandDonnai-Barrow syndrome ()
........expandEhlers-Danlos syndrome due to tenascin-X deficiency ()
........expandEhlers-Danlos syndrome, classic type ()
........expandEmanuel syndrome ()
........expandfamilial omphalocele syndrome with facial dysmorphism ()
........expandFryns syndrome ()
........expandKabuki syndrome ()
........expandlethal hydranencephaly-diaphragmatic hernia syndrome ()
........expandlethal omphalocele-cleft palate syndrome ()
........expandlimb body wall complex ()
........expandMatthew-wood syndrome ()
........expandomphalocele syndrome, Shprintzen-Goldberg type ()
........expandomphalocele-diaphragmatic hernia-cardiovascular anomalies-radial ray defect syndrome ()
........expandpentalogy of Cantrell ()
........expandpericardial and diaphragmatic defect ()
........expandSimpson-Golabi-Behmel syndrome ()
........expandSpigelian hernia-cryptorchidism syndrome ()
........expandtetrasomy 12p ()
........expandtrisomy 13 ()
........expandtrisomy 18 ()
........expandWolf-Hirschhorn syndrome ()



 Sister Nodes: 
..expandbladder exstrophy-epispadias-cloacal exstrophy complex ()
..expandnon-syndromic diaphragmatic or abdominal wall malformation ()
..expandsyndromic diaphragmatic or abdominal wall malformation ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:15216
Name:syndromic diaphragmatic or abdominal wall malformation
Definition:A diaphragmatic or abdominal wall malformation that is part of a larger syndrome.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:syndrome associated with diaphragmatic or abdominal wall malformation; syndrome associated with diaphragmatic or abdominal wall malformation; syndromic diaphragmatic or abdominal wall malformation
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
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