MYELOLYMPHATIC INSUFFICIENCY
General Information (adopted from Orphanet):
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Synonyms, Signs:
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PELGER-LIKE ANOMALY WITH LEUKOPENIA AND SUSCEPTIBILITY TO INFECTIONS
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Number of Symptoms
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7
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OrphanetNr:
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OMIM Id:
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310350
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ICD-10:
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UMLs:
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MeSH:
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MedDRA:
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Snomed:
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Prevalence, inheritance and age of onset:
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Prevalence:
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No data available.
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Inheritance:
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X-linked recessive inheritance
[Omim]
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Age of onset:
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Disease classification (adopted from Orphanet):
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Parent Diseases:
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No data available.
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1
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(HPO:0011447)
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Hyposegmentation of neutrophil nuclei |
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3 / 7739
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2
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(HPO:0001882)
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Leukopenia |
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51 / 7739
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3
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(HPO:0002718)
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Recurrent bacterial infections |
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75 / 7739
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4
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(HPO:0004429)
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Recurrent viral infections |
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20 / 7739
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5
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(OMIM)
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Susceptibility to bacterial and viral infections |
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1 / 7739
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6
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(OMIM)
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Myelolymphatic insufficiency |
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1 / 7739
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7
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(HPO:0001419)
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X-linked recessive inheritance |
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189 / 7739
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ClinVar (via SNiPA)
| Gene symbol |
Variation |
Clinical significance |
Reference |