Chondrocalcinosis

Symptom Information:

Symptom ID: HPO:0000934
Synonyms:
Chondrocalcinosis [OMIM:Chondrocalcinosis]
Chondrocalcinosis (hypophosphatasia only) [OMIM:Chondrocalcinosis (hypophosphatasia only)]
Chondrocalcinosis [MedDRA:10061761]
Quality:
Cross references:
OMIM: "Chondrocalcinosis" [OMIM:Chondrocalcinosis]
OMIM: "Chondrocalcinosis (hypophosphatasia only)" [OMIM:Chondrocalcinosis (hypophosphatasia only)]
UMLS:C0553730 "Chondrocalcinosis" [HPO:0000934]
Is a (Direct Parents):
HPO         Abnormality of Sharpey fibers
MedDRA Crystal arthropathic disorders
HPO         Ectopic calcification
HPO         Abnormal joint morphology
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of connective tissue(HPO:0003549)
          Abnormality of Sharpey fibers(HPO:0100685)
             Chondrocalcinosis(HPO:0000934)
       Abnormality of the skeletal system(HPO:0000924)
          Ectopic calcification(HPO:0010766)
             Chondrocalcinosis(HPO:0000934)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal joint morphology(HPO:0001367)
                Chondrocalcinosis(HPO:0000934)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Joint disorders(MedDRA:10023213)
       Crystal arthropathic disorders(MedDRA:10011505)
          Chondrocalcinosis(HPO:0000934)
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

Adult hypophosphatasia (Orphanet:247676)
BARTTER SYNDROME, ANTENATAL, TYPE 1 (OMIM:601678)
BARTTER SYNDROME, ANTENATAL, TYPE 2 (OMIM:241200)
Bartter syndrome (Orphanet:112)
CHONDROCALCINOSIS 1 (OMIM:600668)
CHONDROCALCINOSIS DUE TO APATITE CRYSTAL DEPOSITION (OMIM:118610)
Familial hypocalciuric hypercalcemia type 2 (Orphanet:101049)
Familial hypocalciuric hypercalcemia type 3 (Orphanet:101050)
Gitelman syndrome (Orphanet:358)
Menkes disease (Orphanet:565)
Odontohypophosphatasia (Orphanet:247685)
Werner syndrome (Orphanet:902)
Wilson disease (Orphanet:905)