Vitamin K deficiency

Symptom Information:

Symptom ID: HPO:0011892
Synonyms:
Vitamin K deficiency (disorder) [Orphanet:49860]
Vitamin K Deficiency [Orphanet:49860]
Vitamin K deficiency [OMIM:Vitamin K deficiency]
Vitamin K/K1/K2 deficiency [Orphanet:49860]
Vitamin K deficiency [Orphanet:49860]
Vitamin K deficiency [MedDRA:10047634]
Deficiency of vitamin K [MedDRA:10047634]
Phytonadione deficiency [MedDRA:10047634]
Quality:
Cross references:
HPO:0100831 "Abnormality of vitamin K metabolism" [Orphanet:49860]
Orphanet:49860 "Vitamin K/K1/K2 deficiency" [Orphanet:49860]
OMIM: "Vitamin K deficiency" [OMIM:Vitamin K deficiency]
UMLS:C0042880 "Vitamin K Deficiency" [Orphanet:49860]
Is a (Direct Parents):
HPO         Abnormality of vitamin K metabolism
MedDRA Fat soluble vitamin deficiencies and disorders
Orphanet Abnormality of vitamin metabolism
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)
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)