Abnormality of the adrenal glands

Symptom Information:

Symptom ID: HPO:0000834
Synonyms:
Adrenal abnormalities [HPO:0000834]
Adrenal gland disease [HPO:0000834]
Adrenal gland anomaly [Orphanet:41390]
Congenital anomaly of adrenal gland (disorder) [Orphanet:41390]
Congenital anomaly of adrenal gland [Orphanet:41390]
Adrenal glands anomalies [Orphanet:41390]
Congenital anomaly of adrenal gland [MedDRA:10062341]
Anomalies of adrenal gland, congenital [MedDRA:10062341]
Congenital adrenal gland anomaly NOS [MedDRA:10062341]
Congenital anomalies of adrenal gland [MedDRA:10062341]
Quality:
Cross references:
Orphanet:41390 "Adrenal glands anomalies" [Orphanet:41390]
UMLS:C0158797 "Congenital anomaly of adrenal gland" [Orphanet:41390]
Is a (Direct Parents):
Orphanet Abnormality of the endocrine system
HPO         Abnormality of the endocrine system
MedDRA Adrenal gland disorders NEC
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)
MedDRA:
Endocrine disorders(MedDRA:10014698)
    Adrenal gland disorders(MedDRA:10001353)
       Adrenal gland disorders NEC(MedDRA:10001354)
          Abnormality of the adrenal glands(HPO:0000834)
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

Adrenomyodystrophy (Orphanet:977)
Beckwith-Wiedemann syndrome (Orphanet:116)
CHARGE syndrome (Orphanet:138)
CHILD syndrome (Orphanet:139)
Catecholamine-producing tumor (Orphanet:717)
Cholesteryl ester storage disease (Orphanet:75234)
Fetal brain disruption sequence (Orphanet:1665)
IMAGe syndrome (Orphanet:85173)
Lethal restrictive dermopathy (Orphanet:1662)
Myopathy - growth delay - intellectual deficit - hypospadias (Orphanet:2601)
Primary pigmented nodular adrenocortical disease (Orphanet:189439)
Rothmund-Thomson syndrome (Orphanet:2909)
Treacher-Collins syndrome (Orphanet:861)
Wolman disease (Orphanet:75233)