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Parent Node:
expandmultiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome (MONDO:0015160)
..Starting node
..expandgenetic multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome ()

       Child Nodes:
........expand22q11.2 deletion syndrome ()
........expandablepharon macrostomia syndrome ()
........expandacromegaloid facial appearance syndrome ()
........expandanophthalmia/microphthalmia-esophageal atresia syndrome ()
........expandAntley-Bixler syndrome ()
........expandarachnodactyly-intellectual disability-dysmorphism syndrome ()
........expandautosomal dominant popliteal pterygium syndrome ()
........expandautosomal dominant primary microcephaly ()
........expandBardet-Biedl syndrome ()
........expandBrachymorphism-onychodysplasia-dysphalangism syndrome ()
........expandbranchiogenic deafness syndrome ()
........expandcampomelia, Cumming type ()
........expandcampomelic dysplasia ()
........expandCarey-Fineman-Ziter syndrome ()
........expandcerebrocostomandibular syndrome ()
........expandChar syndrome ()
........expandCHARGE syndrome ()
........expandchromosome 1p32-p31 deletion syndrome ()
........expandcombined immunodeficiency with faciooculoskeletal anomalies ()
........expandcontractures-developmental delay-Pierre Robin syndrome ()
........expandcurry-Jones syndrome ()
........expandDonnai-Barrow syndrome ()
........expanddysmorphism-conductive hearing loss-heart defect syndrome ()
........expandFeingold syndrome ()
........expandfocal dermal hypoplasia ()
........expandfrontometaphyseal dysplasia ()
........expandGoodman syndrome ()
........expandHallermann-Streiff syndrome ()
........expandHennekam-Beemer syndrome ()
........expandhydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome ()
........expandhypertrichotic osteochondrodysplasia Cantu type ()
........expandhypoglossia-hypodactyly syndrome ()
........expandhypomandibular faciocranial dysostosis ()
........expandisotretinoin-like syndrome ()
........expandJoubert syndrome with hepatic defect ()
........expandKallmann syndrome-heart disease syndrome ()
........expandlethal faciocardiomelic dysplasia ()
........expandlethal restrictive dermopathy ()
........expandMarshall-Smith syndrome ()
........expandMeier-Gorlin syndrome ()
........expandmicrophthalmia with limb anomalies ()
........expandmicrophthalmia, Lenz type ()
........expandMietens syndrome ()
........expandMobius syndrome ()
........expandmoyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome ()
........expandNance-Horan syndrome ()
........expandNoonan syndrome-like disorder with loose anagen hair ()
........expandoccipital horn syndrome ()
........expandoculodentodigital dysplasia ()
........expandoculotrichoanal syndrome ()
........expandPallister-hall syndrome ()
........expandPHACE syndrome ()
........expandpolyvalvular heart disease syndrome ()
........expandPotocki-Shaffer syndrome ()
........expandPrader-Willi syndrome ()
........expandPrader-Willi-like syndrome ()
........expandRobinow-like syndrome ()
........expandSchinzel-Giedion syndrome ()
........expandshort stature-wormian bones-dextrocardia syndrome ()
........expandSHORT syndrome ()
........expandSilver-Russell syndrome ()
........expandsplit hand-foot malformation 3 ()
........expandsymptomatic form of Coffin-Lowry syndrome in female carriers ()
........expandTELO2-related intellectual disability-neurodevelopmental disorder ()
........expandToriello-Carey syndrome ()
........expandulnar-mammary syndrome ()



 Sister Nodes: 
..expandgenetic multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome ()
..expandmicrogastria-limb reduction defect syndrome ()
..expandshort stature-heart defect-craniofacial anomalies syndrome ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:43007
Name:genetic multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
Definition:An instance of multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome that is caused by an inherited modification of the individual's genome.
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TreeNumbers:
Synonyms:genetic MCA/variable MR; genetic multiple congenital anomalies-variable intellectual disability with or without dysmorphism syndrome; hereditary multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
Slim Mappings:
Reference: MedGen:
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OMIM:
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Phenotypes
Disease Causing ClinVar Variants
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