PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4
General Information (adopted from Orphanet):
Synonyms, Signs: |
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Number of Symptoms | 14 |
OrphanetNr: | |
OMIM Id: |
615830
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ICD-10: |
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UMLs: |
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MeSH: |
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MedDRA: |
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Snomed: |
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Prevalence, inheritance and age of onset:
Prevalence: | No data available. |
Inheritance: |
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Age of onset: |
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Disease classification (adopted from Orphanet):
Parent Diseases: | No data available. |
Symptom Information:
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(HPO:0000712) | Emotional lability | 44 / 7739 | ||||
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(HPO:0000819) | Diabetes mellitus | 131 / 7739 | ||||
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(HPO:0008221) | Adrenal hyperplasia | 24 / 7739 | ||||
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(HPO:0001579) | Primary hypercorticolism | 5 / 7739 | ||||
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(HPO:0000939) | Osteoporosis | 129 / 7739 | ||||
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(HPO:0000938) | Osteopenia | 138 / 7739 | ||||
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(HPO:0004324) | Increased body weight | 4 / 7739 | ||||
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(HPO:0001596) | Alopecia | 162 / 7739 | ||||
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(HPO:0000978) | Bruising susceptibility | 123 / 7739 | ||||
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(HPO:0001030) | Fragile skin | 25 / 7739 | ||||
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(HPO:0001061) | Acne | 33 / 7739 | ||||
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(HPO:0001007) | Hirsutism | 91 / 7739 | ||||
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(HPO:0000822) | Hypertension | 224 / 7739 | ||||
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(HPO:0003701) | Proximal muscle weakness | 105 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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