C0008626 |
Congenital chromosomal disease |
ICD10 |
Chromosomal abnormality, unspecified
|
Q99.9 |
C0008626 |
Congenital chromosomal disease |
ICD10CM |
Chromosomal abnormality, unspecified
|
Q99.9 |
C0008626 |
Congenital chromosomal disease |
ICD9CM |
Chromosomal anomalies
|
758 |
C0008626 |
Congenital chromosomal disease |
ICD9CM |
Conditions due to anomaly of unspecified chromosome
|
758.9 |
C0008626 |
Congenital chromosomal disease |
ICD9CM |
Chromosome anomaly NOS
|
758.9 |
C0008626 |
Congenital chromosomal disease |
MONDO |
chromosomal anomaly
|
0019040 |
C0008626 |
Congenital chromosomal disease |
MSH |
Chromosomal Disorders
|
D025063 |
C0008626 |
Congenital chromosomal disease |
MSH |
Chromosome Disorders
|
D025063 |
C0008626 |
Congenital chromosomal disease |
MSH |
Autosomal Chromosome Disorders
|
D025063 |
C0008626 |
Congenital chromosomal disease |
NCI |
Chromosome Abnormality Disorder
|
C34470 |
C0008626 |
Congenital chromosomal disease |
NCI |
Chromosome Disorder
|
C34470 |
C0008626 |
Congenital chromosomal disease |
ORDO |
Rare chromosomal anomaly
|
68335 |