Aplasia/Hypoplasia of the middle phalanx of the 5th finger

Symptom Information:

Symptom ID: HPO:0009161
Synonyms:
Absent/hypoplastic middle phalanx of 5th finger [HPO:0009161]
Absent/hypoplastic middle phalanx of 5th finger [OMIM:Absent/hypoplastic middle phalanx of 5th finger]
Quality:
Cross references:
OMIM: "Absent/hypoplastic middle phalanx of 5th finger" [OMIM:Absent/hypoplastic middle phalanx of 5th finger]
Is a (Direct Parents):
HPO         Abnormality of the middle phalanx of the 5th finger
HPO         Aplasia/Hypoplasia of the phalanges of the 5th finger
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)
                               Abnormality of the phalanges of the 5th finger(HPO:0004213)
                                  Aplasia/Hypoplasia of the phalanges of the 5th finger(HPO:0009376)
                                     Aplasia/Hypoplasia of the middle phalanx of the 5th finger(HPO:0009161)
                                  Abnormality of the middle phalanx of the 5th finger(HPO:0004219)
                                     Aplasia/Hypoplasia of the middle phalanx of the 5th finger(HPO:0009161)
                               Aplasia/Hypoplasia of the phalanges of the hand(HPO:0009767)
                                  Aplasia/Hypoplasia of the phalanges of the 5th finger(HPO:0009376)
                                     Aplasia/Hypoplasia of the middle phalanx of the 5th finger(HPO:0009161)
                            Abnormality of the 5th finger(HPO:0004207)
                               Abnormality of the phalanges of the 5th finger(HPO:0004213)
                                  Aplasia/Hypoplasia of the phalanges of the 5th finger(HPO:0009376)
                                     Aplasia/Hypoplasia of the middle phalanx of the 5th finger(HPO:0009161)
                                  Abnormality of the middle phalanx of the 5th finger(HPO:0004219)
                                     Aplasia/Hypoplasia of the middle phalanx of the 5th finger(HPO:0009161)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of finger(HPO:0001167)
                         Abnormality of phalanx of finger(HPO:0005918)
                            Abnormality of the phalanges of the 5th finger(HPO:0004213)
                               Aplasia/Hypoplasia of the phalanges of the 5th finger(HPO:0009376)
                                  Aplasia/Hypoplasia of the middle phalanx of the 5th finger(HPO:0009161)
                               Abnormality of the middle phalanx of the 5th finger(HPO:0004219)
                                  Aplasia/Hypoplasia of the middle phalanx of the 5th finger(HPO:0009161)
                            Aplasia/Hypoplasia of the phalanges of the hand(HPO:0009767)
                               Aplasia/Hypoplasia of the phalanges of the 5th finger(HPO:0009376)
                                  Aplasia/Hypoplasia of the middle phalanx of the 5th finger(HPO:0009161)
                         Abnormality of the 5th finger(HPO:0004207)
                            Abnormality of the phalanges of the 5th finger(HPO:0004213)
                               Aplasia/Hypoplasia of the phalanges of the 5th finger(HPO:0009376)
                                  Aplasia/Hypoplasia of the middle phalanx of the 5th finger(HPO:0009161)
                               Abnormality of the middle phalanx of the 5th finger(HPO:0004219)
                                  Aplasia/Hypoplasia of the middle phalanx of the 5th finger(HPO:0009161)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Brachydactyly type A2 (Orphanet:93396)
FEINGOLD SYNDROME 1 (OMIM:164280)
Feingold syndrome (Orphanet:1305)
Mesoaxial synostotic syndactyly with phalangeal reduction (Orphanet:157801)