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Term:
autosomal anomaly
(EFO:MONDO:0020049)
Annotations:
Rat: (0)
Mouse: (0)
Human: (0)
Chinchilla: (0)
Bonobo: (0)
Dog: (0)
Squirrel: (0)
Pig: (0)
Naked Mole-rat: (0)
Green Monkey: (0)
Parent Terms
Term With Siblings
Child Terms
chromosomal disorder
+
aneuploidy
+
autosomal anomaly
+
Chromosomal disorder in which the chromosomal anomaly involves an autosome.
Bloom syndrome
chromosome 1p36 deletion syndrome, proximal
duplication/inversion 15q11
gonosome anomaly
+
mosaic variegated aneuploidy syndrome
+
polyploidy
+
Prader-Willi syndrome
+
ring chromosome disorder
+
Silver-Russell syndrome
+
syndrome caused by partial chromosomal deletion
+
syndrome caused by partial chromosomal duplication
+
uniparental disomy
+
chromosome 1 disorder
+
chromosome 10 disorder
+
chromosome 11 disorder
+
chromosome 12 disorder
+
chromosome 13 disorder
+
chromosome 14 disorder
+
chromosome 15 disorder
+
chromosome 16 disorder
+
chromosome 17 disorder
+
chromosome 18 disorder
+
chromosome 19 disorder
+
chromosome 2 disorder
+
chromosome 20 disorder
+
chromosome 21 disorder
+
chromosome 22 disorder
+
chromosome 3 disorder
+
chromosome 4 disorder
+
chromosome 5 disorder
+
chromosome 6 disorder
+
chromosome 7 disorder
+
chromosome 8 disorder
+
chromosome 9 disorder
+
Synonyms
Exact Synonyms:
autosome chromosomal anomaly ; chromosomal anomaly of autosome
Alternate IDs:
MONDO:0020049
Xrefs:
GARD:19417
; MEDGEN:1843454 ;
ORDO:98127
; UMLS:C5681496
External Ontologys:
disease_has_location EFO:GO:0030849
Definition Sources:
MONDO:patterns/location