Deficiency or absence of p47-phox protein (type I)
Symptom Information:
Symptom ID:
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OMIM : No Id available
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Synonyms:
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Quality:
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Cross references:
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OMIM: "Deficiency or absence of p47-phox protein (type I)" [OMIM:Deficiency or absence of p47-phox protein (type I)] |
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Is a (Direct Parents):
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Is a (Whole tree):
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HPO:
MedDRA:
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Database Frequency:
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1 / 7739
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Resource:
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All diseases associated with this symptom:
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE I
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(OMIM:233700)
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