Calcinosis
Symptom Information:
Symptom ID: | HPO:0003761 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the musculature(HPO:0003011) Abnormality of muscle morphology(HPO:0011805) Calcinosis(HPO:0003761) MedDRA: General disorders and administration site conditions(MedDRA:10018065) Tissue disorders NEC(MedDRA:10007867) Trophic disorders(MedDRA:10044694) Calcinosis(HPO:0003761) |
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Database Frequency: | 12 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Arthrogryposis multiplex congenita - whistling face | (Orphanet:1150) |
CREST syndrome | (Orphanet:90290) |
Diffuse cutaneous systemic sclerosis | (Orphanet:220393) |
Hypercalcemic tumoral calcinosis | (Orphanet:306661) |
Limited cutaneous systemic sclerosis | (Orphanet:220402) |
Limited systemic sclerosis | (Orphanet:220407) |
Mandibuloacral dysplasia | (Orphanet:2457) |
Neonatal severe primary hyperparathyroidism | (Orphanet:417) |
Normocalcemic tumoral calcinosis | (Orphanet:306658) |
Pediatric systemic sclerosis | (Orphanet:93567) |
Reynolds syndrome | (Orphanet:779) |
Systemic sclerosis | (Orphanet:90291) |