Short 3rd metacarpal

Symptom Information:

Symptom ID: HPO:0010041
Synonyms:
Hypoplastic 3rd metacarpal [HPO:0010041]
Short third metacarpals [HPO:0010041]
Small 3rd metacarpals [HPO:0010041]
Short 3rd metacarpals [OMIM:Short 3rd metacarpals]
Quality:
Cross references:
OMIM: "Short 3rd metacarpals" [OMIM:Short 3rd metacarpals]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of the 3rd 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)
                            Short metacarpal(HPO:0010049)
                               Short 3rd metacarpal(HPO:0010041)
                            Aplasia/Hypoplasia of the 3rd metacarpal(HPO:0010039)
                               Short 3rd metacarpal(HPO:0010041)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   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)
                               Short metacarpal(HPO:0010049)
                                  Short 3rd metacarpal(HPO:0010041)
                               Aplasia/Hypoplasia of the 3rd metacarpal(HPO:0010039)
                                  Short 3rd metacarpal(HPO:0010041)
                      Abnormality of the hand(HPO:0001155)
                         Abnormality of the metacarpal bones(HPO:0001163)
                            Abnormality of the 3rd metacarpal(HPO:0010011)
                               Aplasia/Hypoplasia of the 3rd metacarpal(HPO:0010039)
                                  Short 3rd metacarpal(HPO:0010041)
                            Abnormal metacarpal morphology(HPO:0005916)
                               Aplasia/Hypoplasia involving the metacarpal bones(HPO:0005914)
                                  Short metacarpal(HPO:0010049)
                                     Short 3rd metacarpal(HPO:0010041)
                                  Aplasia/Hypoplasia of the 3rd metacarpal(HPO:0010039)
                                     Short 3rd metacarpal(HPO:0010041)
                         Aplasia/hypoplasia involving bones of the hand(HPO:0005927)
                            Aplasia/Hypoplasia involving the metacarpal bones(HPO:0005914)
                               Short metacarpal(HPO:0010049)
                                  Short 3rd metacarpal(HPO:0010041)
                               Aplasia/Hypoplasia of the 3rd metacarpal(HPO:0010039)
                                  Short 3rd metacarpal(HPO:0010041)
                   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)
                               Short metacarpal(HPO:0010049)
                                  Short 3rd metacarpal(HPO:0010041)
                               Aplasia/Hypoplasia of the 3rd metacarpal(HPO:0010039)
                                  Short 3rd metacarpal(HPO:0010041)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Chondrodysplasia punctata, tibial-metacarpal type (Orphanet:79346)
Keipert syndrome (Orphanet:2662)
Otopalatodigital syndrome type 1 (Orphanet:90650)
PELGER-HUET ANOMALY (OMIM:169400)
Roifman syndrome (Orphanet:353298)