Megaloblastic anemia
Symptom Information:
Symptom ID: | HPO:0001889 | |||||||||||||||
Synonyms: |
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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 blood and blood-forming tissues(HPO:0001871) Abnormality of erythrocytes(HPO:0001877) Anemia(HPO:0001903) Anemia of inadequate production(HPO:0010972) Macrocytic anemia(HPO:0001972) Megaloblastic anemia(HPO:0001889) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Vitamin related disorders(MedDRA:10047635) Vitamin deficiencies NEC(MedDRA:10047627) Megaloblastic anemia(HPO:0001889) |
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Database Frequency: | 28 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
3-phosphoglycerate dehydrogenase deficiency | (Orphanet:79351) |
Acute erythroid leukemia | (Orphanet:318) |
Congenital intrinsic factor deficiency | (Orphanet:332) |
Constitutional megaloblastic anemia with severe neurologic disease | (Orphanet:319651) |
Cystic fibrosis - gastritis - megaloblastic anemia | (Orphanet:2575) |
Formiminoglutamic aciduria | (Orphanet:51208) |
Gräsbeck-Imerslund disease | (Orphanet:35858) |
Hereditary folate malabsorption | (Orphanet:90045) |
Hereditary orotic aciduria | (Orphanet:30) |
Homocystinuria without methylmalonic aciduria | (Orphanet:622) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
INTRINSIC FACTOR AND R BINDER, COMBINED CONGENITAL DEFICIENCY OF | (OMIM:243320) |
INTRINSIC FACTOR DEFICIENCY | (OMIM:261000) |
LESCH-NYHAN SYNDROME | (OMIM:300322) |
Lesch-Nyhan syndrome | (Orphanet:510) |
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) |
PERNICIOUS ANEMIA | (OMIM:170900) |
Permanent neonatal diabetes mellitus | (Orphanet:99885) |
Thiamine-responsive megaloblastic anemia syndrome | (Orphanet:49827) |
Vitamin B12-responsive methylmalonic acidemia, type cblDv2 | (Orphanet:308442) |
Wolfram syndrome 1 | (OMIM:222300) |
Wolfram syndrome, mitochondrial form | (OMIM:598500) |