Short 2nd metacarpal

Symptom Information:

Symptom ID: HPO:0010038
Synonyms:
Hypoplastic 2nd metacarpal [HPO:0010038]
Rudimentary 2nd metacarpal [HPO:0010038]
Rudimentary 2nd metacarpal [OMIM:Rudimentary 2nd metacarpal]
Quality:
Cross references:
OMIM: "Rudimentary 2nd metacarpal" [OMIM:Rudimentary 2nd metacarpal]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of the 2nd metacarpal
HPO         Short metacarpal
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)
             Aplasia/hypoplasia involving the skeleton(HPO:0009115)
                Aplasia/hypoplasia of the extremities(HPO:0009815)
                   Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                      Aplasia/hypoplasia involving bones of the hand(HPO:0005927)
                         Aplasia/Hypoplasia involving the metacarpal bones(HPO:0005914)
                            Aplasia/Hypoplasia of the 2nd metacarpal(HPO:0010036)
                               Short 2nd metacarpal(HPO:0010038)
                            Short metacarpal(HPO:0010049)
                               Short 2nd metacarpal(HPO:0010038)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Aplasia/hypoplasia of the extremities(HPO:0009815)
                      Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                         Aplasia/hypoplasia involving bones of the hand(HPO:0005927)
                            Aplasia/Hypoplasia involving the metacarpal bones(HPO:0005914)
                               Aplasia/Hypoplasia of the 2nd metacarpal(HPO:0010036)
                                  Short 2nd metacarpal(HPO:0010038)
                               Short metacarpal(HPO:0010049)
                                  Short 2nd metacarpal(HPO:0010038)
                   Abnormality of the upper limb(HPO:0002817)
                      Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                         Aplasia/hypoplasia involving bones of the hand(HPO:0005927)
                            Aplasia/Hypoplasia involving the metacarpal bones(HPO:0005914)
                               Aplasia/Hypoplasia of the 2nd metacarpal(HPO:0010036)
                                  Short 2nd metacarpal(HPO:0010038)
                               Short metacarpal(HPO:0010049)
                                  Short 2nd metacarpal(HPO:0010038)
                      Abnormality of the hand(HPO:0001155)
                         Abnormality of the metacarpal bones(HPO:0001163)
                            Abnormality of the 2nd metacarpal(HPO:0010010)
                               Aplasia/Hypoplasia of the 2nd metacarpal(HPO:0010036)
                                  Short 2nd metacarpal(HPO:0010038)
                            Abnormal metacarpal morphology(HPO:0005916)
                               Aplasia/Hypoplasia involving the metacarpal bones(HPO:0005914)
                                  Aplasia/Hypoplasia of the 2nd metacarpal(HPO:0010036)
                                     Short 2nd metacarpal(HPO:0010038)
                                  Short metacarpal(HPO:0010049)
                                     Short 2nd metacarpal(HPO:0010038)
                         Aplasia/hypoplasia involving bones of the hand(HPO:0005927)
                            Aplasia/Hypoplasia involving the metacarpal bones(HPO:0005914)
                               Aplasia/Hypoplasia of the 2nd metacarpal(HPO:0010036)
                                  Short 2nd metacarpal(HPO:0010038)
                               Short metacarpal(HPO:0010049)
                                  Short 2nd metacarpal(HPO:0010038)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Chondrodysplasia punctata, tibial-metacarpal type (Orphanet:79346)
Phocomelia - ectrodactyly - deafness - sinus arrhythmia (Orphanet:2878)