Calcinosis

Symptom Information:

Symptom ID: HPO:0003761
Synonyms:
Calcinosis [OMIM:Calcinosis]
Calcinosis [MedDRA:10006938]
Quality:
Cross references:
OMIM: "Calcinosis" [OMIM:Calcinosis]
UMLS:C0006663 "Calcinosis" [HPO:0003761]
Is a (Direct Parents):
HPO         Abnormality of muscle morphology
MedDRA Trophic disorders
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)
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)