Vitamin K deficiency
Symptom Information:
Symptom ID: | HPO:0011892 | ||||||||
Synonyms: |
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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 metabolism/homeostasis(HPO:0001939) Abnormality of vitamin metabolism(HPO:0100508) Abnormality of vitamin K metabolism(HPO:0100831) Vitamin K deficiency(HPO:0011892) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Vitamin related disorders(MedDRA:10047635) Fat soluble vitamin deficiencies and disorders(MedDRA:10016250) Vitamin K deficiency(HPO:0011892) |
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Database Frequency: | 4 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant chondrodysplasia punctata | (Orphanet:79344) |
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
Familial hypercholanemia | (Orphanet:238475) |
Maxillo-nasal dysplasia | (Orphanet:1248) |