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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
chromosomal disease +     
16Q24.3 Microdeletion Syndrome  
6q+ Syndrome, Partial 
7p2 Monosomy Syndrome 
9q22.3 Microdeletion 
Angelman syndrome  
Beckwith-Wiedemann syndrome +   
branchiootorenal syndrome +   
chromosomal duplication syndrome +   
Chromosome 13q-Mosaicism 
Chromosome 22, Monosome Mosaic 
Chromosome 4, 4q Terminal Deletion Syndrome 
Chromosome 6 Ring Syndrome 
Chromosome 7 Ring Syndrome 
Chromosome Deletion +   
Cornelia de Lange syndrome +   
deafness, dystonia, and cerebral hypomyelination  
Delayed Cranial Ossification due to CBFB Haploinsufficiency 
Deletion 13q Syndrome, Partial 
Distal Trisomy 10q Syndrome 
Duplication 4p Syndrome 
Edinburgh Malformation Syndrome 
Emanuel Syndrome 
holoprosencephaly +   
Intellectual Developmental Disorder, Autosomal Dominant, FRA12A Type  
Isodicentric Chromosome 15 Syndrome  
mosaic variegated aneuploidy syndrome +   
Pallister Killian Syndrome  
Partial Duplication 15q Syndrome 
Partial Trisomy 3q Syndrome 
Prader-Willi syndrome +   
Recombinant Chromosome 8 Syndrome  
Ring Chromosome 4 Syndrome 
ring chromosome syndrome +   
Schmid-Fraccaro Syndrome  
Sex Chromosome Disorders +   
Silver-Russell syndrome +   
Sotos syndrome +   
Thrombocytopenia 2  
Trisomy 18-Like Syndrome 
Warburton Anyane Yeboa Syndrome  

Synonyms
Exact Synonyms: Chromosome 22 mosaic monosomy ;   Mosaic Monosome 22
Primary IDs: MESH:C536798 ;   RDO:0002489

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