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adrenocorticotropic hormone deficiency (DOID:0080150)
Annotations: Rat: (2) Mouse: (2) Human: (2) Chinchilla: (2) Bonobo: (1) Dog: (2) Squirrel: (2) Pig: (2)
Parent Terms Term With Siblings Child Terms
genetic disease +     
hypoglycemia +     
hypopituitarism +     
3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency  
Addison's disease +   
Adrenocortical Hypofunction, Chronic Primary Congenital 
Adrenocortical Insufficiency  
adrenocorticotropic hormone deficiency  
A hypopituitarrium that is characterized by a decreased or absent production of adrenocorticotropic hormone by the pituitary gland. (DO)
adrenoleukodystrophy +   
advanced sleep phase syndrome 3  
age related macular degeneration 8  
Alagille syndrome  
Alpha-2-Deficient Collagen Disease 
Aquaporin 1 Deficiency 
ataxic cerebral palsy 
atrial heart septal defect 3  
atrial heart septal defect 4  
autoimmune lymphoproliferative syndrome +   
brachydactyly type A1B 
brachydactyly type A1C  
brachydactyly type A1D  
brachydactyly type B1  
brachydactyly type B2  
brachydactyly type E1  
brachydactyly type E2  
carnitine palmitoyltransferase I deficiency  
Carnitine Palmitoyltransferase II Deficiency, Infantile  
cataract 23  
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
Cenani-Lenz syndactyly syndrome  
CHARGE syndrome  
chromosomal disease +   
Combined Pituitary Hormone Deficiency, 5  
complex cortical dysplasia with other brain malformations 1  
complex cortical dysplasia with other brain malformations 2  
complex cortical dysplasia with other brain malformations 3  
complex cortical dysplasia with other brain malformations 4  
complex cortical dysplasia with other brain malformations 5  
complex cortical dysplasia with other brain malformations 6  
Congenital Adrenal Hypoplasia with Absent Pituitary Luteinizing Hormone 
congenital adrenal insufficiency  
Congenital Hepatic Fibrosis  
Congenital Hyperinsulinism +   
Congenital Hypopituitarism with Central Diabetes Insipidus 
Congenital Pain Insensitivity +   
Culler-Jones syndrome  
desquamative interstitial pneumonia  
Dincsoy Salih Patel Syndrome 
Dwarfism +   
Familial Cirrhosis +   
Familial Dysalbuminemic Hyperthyroxinemia  
Familial Hemophagocytic Lymphohistiocytoses +   
familial hypertrophic cardiomyopathy +   
Familial Lipochrome Histiocytosis 
Familial Mixed Cryoglobulinemia  
Familial Temporal Epilepsy +   
frontotemporal dementia and/or amyotrophic lateral sclerosis-3  
frontotemporal dementia and/or amyotrophic lateral sclerosis-4  
Genetic Skin Diseases +   
glucocorticoid deficiency 1  
Glucocorticoid Deficiency 2  
Glucocorticoid Deficiency 3 
Glucocorticoid Deficiency 4  
Glucocorticoid Deficiency 5  
Hereditary Bilateral Parotidomegaly 
Hereditary Epistaxis 
Hereditary Eye Diseases +   
hereditary lymphedema +   
Hereditary Neoplastic Syndromes +   
Hirata disease 
holoprosencephaly 9  
Hypoaldosteronism +   
hypogonadotropic hypogonadism 5 with or without anosmia +   
hypoinsulinemic hypoglycemia with hemihypertrophy  
IMAGe syndrome  
inherited metabolic disorder +   
Insulin Coma 
isolated growth hormone deficiency +   
Isolated Prolactin Deficiency 
Kallmann syndrome +   
Kaplowitz Bodurtha syndrome 
Laminopathies +   
Lennox-Gastaut syndrome  
leucine-sensitive hypoglycemia of infancy  
Marfan syndrome +   
monogenic disease +   
Neonatal Hypoglycemia, Simulating Foetopathia Diabetica  
Nervous System Heredodegenerative Disorders +   
Nonimmune Chronic Idiopathic Neutropenia, Adult  
osteochondrodysplasia +   
panhypopituitarism +   
polygenic disease +   
primary hypertrophic osteoarthropathy +   
progressive familial intrahepatic cholestasis +   
Prolactin Deficiency with Obesity and Enlarged Testes 
Proopiomelanocortin Deficiency  
RHYNS Syndrome  
Sacral Agenesis with Vertebral Anomalies  
Schaaf-Yang syndrome  
Sheehan syndrome 
triple-A syndrome  
Waterhouse-Friderichsen syndrome +  
X-linked adrenal hypoplasia congenita  
yellow nail syndrome +  

Exact Synonyms: ACTH DEFICIENCY ;   IAD ;   isolated ACTH deficiency
Primary IDs: MESH:C535668 ;   MESH:C562707
Alternate IDs: OMIM:201400 ;   RDO:0000917 ;   RDO:0012302
Definition Sources: "DO", "DO"

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