Decreased methylcobalamin
Symptom Information:
Symptom ID: | HPO:0003223 | |||||||||||
Synonyms: |
|
|||||||||||
Quality: | ||||||||||||
Cross references: |
|
|||||||||||
Is a (Direct Parents): |
|
|||||||||||
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 B metabolism(HPO:0004340) Abnormality of vitamin B12 metabolism(HPO:0004341) Decreased methylcobalamin(HPO:0003223) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Vitamin related disorders(MedDRA:10047635) Water soluble vitamin deficiencies(MedDRA:10047842) Decreased methylcobalamin(HPO:0003223) |
|||||||||||
Database Frequency: | 11 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
Chronic diarrhea due to guanylate cyclase 2C overactivity | (Orphanet:314373) |
Methylcobalamin deficiency type cblDv1 | (Orphanet:308380) |
Methylcobalamin deficiency type cblE | (Orphanet:2169) |
Methylcobalamin deficiency type cblG | (Orphanet:2170) |
Methylmalonic acidemia with homocystinuria | (Orphanet:26) |
Methylmalonic acidemia with homocystinuria, type cblC | (Orphanet:79282) |
Methylmalonic acidemia with homocystinuria, type cblD | (Orphanet:79283) |
Methylmalonic acidemia with homocystinuria, type cblF | (Orphanet:79284) |
Methylmalonic acidemia with homocystinuria, type cblJ | (Orphanet:369955) |
Vitamin B12-responsive methylmalonic acidemia, type cblDv2 | (Orphanet:308442) |