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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
disease +     
acute disease +   
animal disease +  
breast disease +   
cancer or benign tumor +   
cardiovascular disease +   
chromosomal disorder +  
Clinical conditions caused by an abnormal chromosome constitution in which there is extra or missing chromosome material (either a whole chromosome or a chromosome segment). (from Thompson et al., Genetics in Medicine, 5th ed, p429)
chronic disease +   
complication +   
connective tissue disease +   
digestive system disease +   
disease related to transplantation +   
disorder of development or morphogenesis +   
disorder of visual system +   
endocrine system disease +   
genetic disorder +   
head and neck disorder +   
hematologic disease +   
iatrogenic disease +  
idiopathic disease +   
immune system disease +   
infectious disease +   
inflammatory disease +   
integumentary system disease +   
metabolic disease +   
mitochondrial disease +  
musculoskeletal system disease +   
nervous system disease +   
obstetric disorder +   
occupational disorder +   
otorhinolaryngologic disease +   
perinatal disease +   
perineum disease 
poisoning +   
post-infectious disorder +   
premature aging syndrome +   
psychiatric disorder +   
radiation-induced disorder +   
reproductive system disease +   
respiratory system disease +   
soft tissue disease  
sudden infant death syndrome +  
syndromic disease +   
ulcer disease +   
upper digestive tract disorder +   
urinary system disease +   
urogenital neoplasm +   

Synonyms
Exact Synonyms: DOID:0080014 ;   NCIT:C34470 ;   Orphanet:68335 ;   chromosomal disease ;   chromosomal disorders ;   chromosome disorder ;   disorders, chromosome ;   http://identifiers.org/medgen/3441 ;   http://identifiers.org/mesh/D025063 ;   http://identifiers.org/snomedct/409709004
Related Synonyms: autosomal chromosome disorder ;   autosomal chromosome disorders ;   chromosome abnormality disorder ;   chromosome abnormality disorders
Alternate IDs: MONDO:0019040
Xrefs: DOID:0080014 ;   ICD10CM:Q90-Q99 ;   ICD9:758.89 ;   MEDGEN:3441 ;   MESH:D025063 ;   NANDO:1100014 ;   NANDO:2100279 ;   NANDO:2100280 ;   NCI:C34470 ;   ORDO:68335
External Ontologys: in_taxon EFO:NCBITaxon:9606
Definition Sources: MESH:D025063

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