MYELOCYTIC LEUKEMIA-LIKE SYNDROME, FAMILIAL, CHRONIC

General Information (adopted from Orphanet):

Synonyms, Signs: CML-LIKE SYNDROME, FAMILIAL
Number of Symptoms 3
OrphanetNr:
OMIM Id: 600080
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0005506) Chronic myelogenous leukemia 3 / 7739
2
 (OMIM) No Philadelphia chromosome 1 / 7739
3
 (OMIM) Familial chronic myelocytic leukemia-like syndrome 1 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: