MYELOPROLIFERATIVE DISEASE, AUTOSOMAL RECESSIVE

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 3
OrphanetNr:
OMIM Id: 254700
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal recessive inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0005547) Myeloproliferative disorder 7 / 7739
2
 (HPO:0004852) Reduced leukocyte alkaline phosphatase 1 / 7739
3
 (HPO:0000007) Autosomal recessive inheritance 2538 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information:

Clinical Description OMIM Randall et al. (1965) observed a severe myeloproliferative disorder with features resembling chronic or subacute myeloid leukemia in 9 children related as first or second cousins. Two children recovered completely after a chronic illness of 10 to 12 ...