Adrenocortical hypoplasia

Symptom Information:

Symptom ID: HPO:0008182
Synonyms:
Adrenocortical insufficiency [Orphanet:41420]
Adrenal cortical hypofunction [Orphanet:41420]
Cortico-adrenal hypoplasia/insufficiency [Orphanet:41420]
Adrenocortical insufficiency (uncommon) [OMIM:Adrenocortical insufficiency (uncommon)]
Adrenal cortical hypofunctions [MedDRA:10001343]
Quality:
Cross references:
HPO:0008207 "Primary adrenal insufficiency" [Orphanet:41420]
HPO:0011735 "Adrenocorticotropin (ACTH) deficient adrenal insufficiency" [Orphanet:41420]
HPO:0000835 "Adrenal hypoplasia" [Orphanet:41420]
HPO:0000846 "Adrenal insufficiency" [Orphanet:41420]
Orphanet:41420 "Cortico-adrenal hypoplasia/insufficiency" [Orphanet:41420]
OMIM: "Adrenocortical insufficiency (uncommon)" [OMIM:Adrenocortical insufficiency (uncommon)]
UMLS:C0405580 "Adrenal cortical hypofunction" [Orphanet:41420]
Is a (Direct Parents):
Orphanet Abnormality of the adrenal glands
MedDRA Adrenal gland disorders
HPO         Adrenocortical abnormality
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the endocrine system(HPO:0000818)
          Abnormality of the adrenal glands(HPO:0000834)
             Abnormality of adrenal morphology(HPO:0011732)
                Adrenocortical abnormality(HPO:0000849)
                   Adrenocortical hypoplasia(HPO:0008182)
MedDRA:
Endocrine disorders(MedDRA:10014698)
    Adrenal gland disorders(MedDRA:10001353)
       Adrenocortical hypoplasia(HPO:0008182)
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Bifunctional enzyme deficiency (Orphanet:300)
Isolated glycerol kinase deficiency (Orphanet:408)
Kearns-Sayre syndrome (Orphanet:480)
MELAS (Orphanet:550)