Familial Gestational Hyperthyroidism
Disease ID: disease_node_14386
Connections displayed (default: 10).
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| Dbxref | MIM:603373, ORDO:99819 |
|---|---|
| Subclassof | DOID_0050736, DOID_7998 |
| Data Source | DOID |
| Doid Label | familial gestational hyperthyroidism |
| Doid Description | A hyperthyroidism that is characterized by promiscuous stimulation of the thyrotropin receptor by the excess chorionic gonadotropin and that has_material_basis_in heterozygous mutation in the gene encoding the thyroid-stimulating hormone receptor (TSHR) on chromosome 14q31. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_14386 |
| Doid Id | DOID_0081102 |
| Label | Familial Gestational Hyperthyroidism |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Hyperthyroidism(ID:disease_node_4167) (Disease)