Dwarfism, Pituitary
Disease ID: disease_node_2624
Connections displayed (default: 10).
Loading graph...
| Dbxref | GARD:12556, ICD10CM:E23.0, ICD9CM:253.3, MESH:D004393, NCI:C34555, ORDO:631, SNOMEDCT_US_2023_03_01:270485009, UMLS_CUI:C0013338 |
|---|---|
| Subclassof | DOID_9406 |
| Data Source | DOID, MESH |
| Synonyms | IGHD, congenital IGHD, congenital isolated GH deficiency, congenital isolated growth hormone deficiency, familial isolated growth hormone deficiency, non-acquired isolated growth hormone deficiency |
| Mesh Id | D004393 |
| Mesh Label | Dwarfism, Pituitary |
| Mesh Subclassof | D004392, D001849, D007018 |
| Doid Label | isolated growth hormone deficiency |
| Doid Description | A hypopituitarism characterized by abnormally low levels, absence or impaired function of growth hormone in the absence of abnormalities in other pituitary hormones. |
| Disease Node Id | disease_node_2624 |
| Doid Id | DOID_0060870 |
| Label | Dwarfism, Pituitary |
- Incoming r'ship
SUBCLASS_OFto/from Isolated Growth Hormone Deficiency Type Iii(ID:disease_node_19696) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Isolated Growth Hormone Deficiency Type Ib(ID:disease_node_19697) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Isolated Growth Hormone Deficiency Type Ia(ID:disease_node_19698) (Disease)