Sclerosis of distal finger phalanx

Symptom Information:

Symptom ID: HPO:0100915
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Abnormality of the distal phalanx of finger
HPO         Sclerosis of finger phalanx
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 upper limb(HPO:0002817)
                      Abnormality of the hand(HPO:0001155)
                         Abnormality of finger(HPO:0001167)
                            Abnormality of phalanx of finger(HPO:0005918)
                               Sclerosis of finger phalanx(HPO:0100899)
                                  Sclerosis of distal finger phalanx(HPO:0100915)
                               Abnormality of the distal phalanx of finger(HPO:0009832)
                                  Sclerosis of distal finger phalanx(HPO:0100915)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of finger(HPO:0001167)
                         Abnormality of phalanx of finger(HPO:0005918)
                            Sclerosis of finger phalanx(HPO:0100899)
                               Sclerosis of distal finger phalanx(HPO:0100915)
                            Abnormality of the distal phalanx of finger(HPO:0009832)
                               Sclerosis of distal finger phalanx(HPO:0100915)
             Abnormal bone structure(HPO:0003330)
                Abnormality of bone mineral density(HPO:0004348)
                   Increased bone mineral density(HPO:0011001)
                      Sclerosis of hand bone(HPO:0004054)
                         Sclerosis of finger phalanx(HPO:0100899)
                            Sclerosis of distal finger phalanx(HPO:0100915)
MedDRA:
Database Frequency: 0 / 7739
Resource:

All diseases associated with this symptom: