Tarsal stippling

Symptom Information:

Symptom ID: HPO:0008131
Synonyms:
Punctate calcifications of tarsals [HPO:0008131]
Punctate tarsal calcification [HPO:0008131]
Punctate calcifications of tarsals [OMIM:Punctate calcifications of tarsals]
Quality:
Cross references:
OMIM: "Punctate calcifications of tarsals" [OMIM:Punctate calcifications of tarsals]
Is a (Direct Parents):
HPO         Sclerosis of foot bone
HPO         Abnormal tarsal ossification
HPO         Ectopic calcification
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the lower limb(HPO:0002814)
                      Abnormality of the foot(HPO:0001760)
                         Abnormal foot bone ossification(HPO:0010675)
                            Abnormal tarsal ossification(HPO:0008369)
                               Tarsal stippling(HPO:0008131)
                         Abnormality of the tarsal bones(HPO:0001850)
                            Abnormal tarsal ossification(HPO:0008369)
                               Tarsal stippling(HPO:0008131)
             Abnormal bone structure(HPO:0003330)
                Abnormal bone ossification(HPO:0011849)
                   Abnormal foot bone ossification(HPO:0010675)
                      Abnormal tarsal ossification(HPO:0008369)
                         Tarsal stippling(HPO:0008131)
                Abnormality of bone mineral density(HPO:0004348)
                   Increased bone mineral density(HPO:0011001)
                      Sclerosis of foot bone(HPO:0100925)
                         Tarsal stippling(HPO:0008131)
          Ectopic calcification(HPO:0010766)
             Tarsal stippling(HPO:0008131)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

X-linked dominant chondrodysplasia punctata (Orphanet:35173)