Aplasia/Hypoplasia of the middle phalanges of the toes

Symptom Information:

Symptom ID: HPO:0010194
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of the phalanges of the toes
HPO         Abnormality of the middle phalanges of the toes
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)
                         Abnormality of toe(HPO:0001780)
                            Abnormality of the phalanges of the toes(HPO:0010161)
                               Abnormality of the middle phalanges of the toes(HPO:0010183)
                                  Aplasia/Hypoplasia of the middle phalanges of the toes(HPO:0010194)
                               Aplasia/Hypoplasia of the phalanges of the toes(HPO:0010173)
                                  Aplasia/Hypoplasia of the middle phalanges of the toes(HPO:0010194)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of toe(HPO:0001780)
                         Abnormality of the phalanges of the toes(HPO:0010161)
                            Abnormality of the middle phalanges of the toes(HPO:0010183)
                               Aplasia/Hypoplasia of the middle phalanges of the toes(HPO:0010194)
                            Aplasia/Hypoplasia of the phalanges of the toes(HPO:0010173)
                               Aplasia/Hypoplasia of the middle phalanges of the toes(HPO:0010194)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Brachydactyly type A2 (Orphanet:93396)
Brachydactyly type B2 (Orphanet:140908)
Carpenter syndrome (Orphanet:65759)
Proximal symphalangism (Orphanet:3250)