Absence of intrinsic factor
Symptom Information:
Symptom ID: | HPO:0005219 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the gastrointestinal tract(HPO:0011024) Abnormality of the stomach(HPO:0002577) Absence of intrinsic factor(HPO:0005219) MedDRA: |
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Database Frequency: | 3 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Congenital intrinsic factor deficiency | (Orphanet:332) |
INTRINSIC FACTOR AND R BINDER, COMBINED CONGENITAL DEFICIENCY OF | (OMIM:243320) |
INTRINSIC FACTOR DEFICIENCY | (OMIM:261000) |