Vitamin D deficiency

Symptom Information:

Symptom ID: HPO:0100512
Synonyms:
Vitamin D deficiency (disorder) [Orphanet:49820]
Vitamin D Deficiency [Orphanet:49820]
Vitamin D deficiency [OMIM:Vitamin D deficiency]
Vitamin D deficiency [Orphanet:49820]
Vitamin D deficiency [MedDRA:10047626]
Unspecified vitamin D deficiency [MedDRA:10047626]
Quality:
Cross references:
Orphanet:49820 "Vitamin D deficiency" [Orphanet:49820]
OMIM: "Vitamin D deficiency" [OMIM:Vitamin D deficiency]
UMLS:C0042870 "Vitamin D Deficiency" [Orphanet:49820]
Is a (Direct Parents):
HPO         Abnormality of vitamin D 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 D metabolism(HPO:0100511)
                Vitamin D deficiency(HPO:0100512)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Vitamin related disorders(MedDRA:10047635)
       Fat soluble vitamin deficiencies and disorders(MedDRA:10016250)
          Vitamin D deficiency(HPO:0100512)
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
Oculocerebrorenal syndrome (Orphanet:534)