Decreased methionine synthase activity
Symptom Information:
Symptom ID: | HPO:0003524 | ||||||
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 metabolism/homeostasis(HPO:0001939) Abnormality of carboxylic acid metabolism(HPO:0004354) Abnormality of amino acid metabolism(HPO:0004337) Abnormality of aspartate family amino acid metabolism(HPO:0010899) Abnormality of methionine metabolism(HPO:0010901) Decreased methionine synthase activity(HPO:0003524) Abnormality of sulfur amino acid metabolism(HPO:0004339) Abnormality of methionine metabolism(HPO:0010901) Decreased methionine synthase activity(HPO:0003524) MedDRA: |
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Database Frequency: | 9 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
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) |