Cytogenetic abnormality

Symptom Information:

Symptom ID: MedDRA:10067477
Synonyms:
Chromosome abnormality [Orphanet:52000]
Chromosomal disorder (disorder) [Orphanet:52000]
Congenital disorder due to abnormality of chromosome number OR structure (disorder) [Orphanet:52000]
Congenital chromosomal disease [Orphanet:52000]
Chromosome Aberrations [Orphanet:52000]
Chromosomal or genetic anomaly [Orphanet:52000]
Chromosome abnormalities [OMIM:Chromosome abnormalities]
Gene abnormality [Orphanet:52000]
Genetic anomaly [Orphanet:52000]
Quality:
Cross references:
Orphanet:52000 "Chromosomal or genetic anomaly" [Orphanet:52000]
OMIM: "Chromosome abnormalities" [OMIM:Chromosome abnormalities]
UMLS:C0008626 "Congenital chromosomal disease" [Orphanet:52000]
UMLS:C0008625 "Chromosome Aberrations" [Orphanet:52000]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Acute erythroid leukemia (Orphanet:318)