| Inbound Relationships | 
Type | 
Active | 
Source | 
Characteristic | 
Refinability | 
Group | 
| X-linked panhypopituitarism | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| X-linked hypoparathyroidism | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Kallman syndrome with heart disease | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Hereditary growth hormone deficiency | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Familial steroid-resistant nephrotic syndrome with adrenal insufficiency | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Sanjad Sakati syndrome | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Intrauterine growth restriction, short stature, early adult-onset diabetes syndrome | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Autosomal semi-dominant severe lipodystrophic laminopathy | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Cell death inducing DFFA like effector C-related familial partial lipodystrophy | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Lipase E, hormone sensitive type-related familial partial lipodystrophy | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Peroxisome proliferator activated receptor gamma-related familial partial lipodystrophy | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| AKT serine/threonine kinase 2-related familial partial lipodystrophy | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| 4H leukodystrophy | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Microcephalic primordial dwarfism, insulin resistance syndrome | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Glucagon receptor-related hyperglucagonemia | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Congenital isolated adrenocorticotropic hormone deficiency | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Alstrom syndrome | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| 46,XX ovarian dysgenesis, short stature syndrome | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Familial hyperaldosteronism type 1 | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Congenital leptin deficiency | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Resistance to thyroid hormone due to mutation in thyroid hormone receptor beta | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Polyendocrine polyneuropathy syndrome | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  | 
| Infantile multisystem neurologic, endocrine, pancreatic disease | 
Is a | 
True | 
Hereditary disorder of endocrine system | 
Inferred relationship | 
Existential restriction modifier | 
  |