Pseudohypoparathyroidism
Disease ID: disease_node_6380
Connections displayed (default: 10).
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| Dbxref | GARD:10758, ICD10CM:E20.1, MESH:D011547, NCI:C99027, SNOMEDCT_US_2023_03_01:190867002, UMLS_CUI:C0033806 |
|---|---|
| Subclassof | DOID_896 |
| Data Source | DOID, MESH |
| Synonyms | PHP |
| Mesh Id | D011547 |
| Mesh Label | Pseudohypoparathyroidism |
| Mesh Subclassof | D008664, D001851, D002128 |
| Doid Label | pseudohypoparathyroidism |
| Doid Description | A metal metabolism disorder that is characterized by end-organ resistance to parathyroid hormone and/or a constellation of symptoms collectively termed Albright’s hereditary osteodystrophy, which include shortening and widening of long bones located_in the hand or located_in the foot along with short stature, obesity, and rounded face. |
| Disease Node Id | disease_node_6380 |
| Doid Id | DOID_4184 |
| Label | Pseudohypoparathyroidism |
- Incoming r'ship
SUBCLASS_OFto/from Pseudopseudohypoparathyroidism(ID:disease_node_6388) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Pseudohypoparathyroidism Type 1C(ID:disease_node_17542) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Pseudohypoparathyroidism Type 1A(ID:disease_node_17541) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Pseudohypoparathyroidism Type 1B(ID:disease_node_17540) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Metal Metabolism, Inborn Errors(ID:disease_node_5173) (Disease)