Congenital Intrinsic Factor Deficiency
Disease ID: disease_node_17077
Connections displayed (default: 10).
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| Dbxref | MIM:261000 |
|---|---|
| Subclassof | DOID_0080015, DOID_0050731 |
| Data Source | DOID |
| Synonyms | hereditary intrinsic factor deficiency |
| Doid Label | congenital intrinsic factor deficiency |
| Doid Description | A vitamin B12 deficiency that is characterized by megaloblastic anemia due to the absence of gastric intrinsic factor which results in abnormal vitamin B12 absorption. |
| Disease Node Id | disease_node_17077 |
| Doid Id | DOID_0050734 |
| Disease Has Basis In | HP_0001197 |
| Label | Congenital Intrinsic Factor Deficiency |
- Outgoing r'ship
SUBCLASS_OFto/from Physical Disorder(ID:disease_node_13159) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Vitamin B 12 Deficiency(ID:disease_node_7896) (Disease)