Short third metatarsal

Symptom Information:

Symptom ID: HPO:0004686
Synonyms:
Hypoplasia of the 3rd metatarsal bone [HPO:0004686]
Short metatarsal [Orphanet:22360]
Malimplantation of toes [Orphanet:22360]
Short metatarsals (1 patient) [OMIM:Short metatarsals (1 patient)]
Short metatarsals (4th) [OMIM:Short metatarsals (4th)]
Short metatarsals (4th-5th) [OMIM:Short metatarsals (4th-5th)]
Short metatarsals (especially 4th and 5th) [OMIM:Short metatarsals (especially 4th and 5th)]
Short metatarsals (especially first metatarsal) [OMIM:Short metatarsals (especially first metatarsal)]
Quality:
Cross references:
HPO:0010743 "Short metatarsal bone" [Orphanet:22360]
Orphanet:22360 "Malimplantation of toes" [Orphanet:22360]
OMIM: "Short metatarsals (1 patient)" [OMIM:Short metatarsals (1 patient)]
OMIM: "Short metatarsals (4th)" [OMIM:Short metatarsals (4th)]
OMIM: "Short metatarsals (4th-5th)" [OMIM:Short metatarsals (4th-5th)]
OMIM: "Short metatarsals (especially 4th and 5th)" [OMIM:Short metatarsals (especially 4th and 5th)]
OMIM: "Short metatarsals (especially first metatarsal)" [OMIM:Short metatarsals (especially first metatarsal)]
Is a (Direct Parents):
HPO         Abnormality of the third metatarsal bone
HPO         Short metatarsal
Orphanet Abnormality of the foot
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)
                      Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493)
                         Aplasia/Hypoplasia involving bones of the feet(HPO:0006494)
                            Aplasia/Hypoplasia of metatarsal bones(HPO:0001964)
                               Short metatarsal(HPO:0010743)
                                  Short third metatarsal(HPO:0004686)
                      Abnormality of the foot(HPO:0001760)
                         Abnormality of the metatarsal bones(HPO:0001832)
                            Aplasia/Hypoplasia of metatarsal bones(HPO:0001964)
                               Short metatarsal(HPO:0010743)
                                  Short third metatarsal(HPO:0004686)
                            Abnormality of the third metatarsal bone(HPO:0010672)
                               Short third metatarsal(HPO:0004686)
                         Aplasia/Hypoplasia involving bones of the feet(HPO:0006494)
                            Aplasia/Hypoplasia of metatarsal bones(HPO:0001964)
                               Short metatarsal(HPO:0010743)
                                  Short third metatarsal(HPO:0004686)
                   Aplasia/hypoplasia of the extremities(HPO:0009815)
                      Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493)
                         Aplasia/Hypoplasia involving bones of the feet(HPO:0006494)
                            Aplasia/Hypoplasia of metatarsal bones(HPO:0001964)
                               Short metatarsal(HPO:0010743)
                                  Short third metatarsal(HPO:0004686)
             Abnormality of long bone morphology(HPO:0011314)
                Short long bone(HPO:0003026)
                   Short metatarsal(HPO:0010743)
                      Short third metatarsal(HPO:0004686)
             Aplasia/hypoplasia involving the skeleton(HPO:0009115)
                Aplasia/hypoplasia of the extremities(HPO:0009815)
                   Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493)
                      Aplasia/Hypoplasia involving bones of the feet(HPO:0006494)
                         Aplasia/Hypoplasia of metatarsal bones(HPO:0001964)
                            Short metatarsal(HPO:0010743)
                               Short third metatarsal(HPO:0004686)
MedDRA:
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Femoral-facial syndrome (Orphanet:1988)
Fibular aplasia - complex brachydactyly (Orphanet:2639)
Pseudohypoparathyroidism type 1A (Orphanet:79443)
Pseudohypoparathyroidism type 1C (Orphanet:79444)
Pseudopseudohypoparathyroidism (Orphanet:79445)
SATOYOSHI SYNDROME (OMIM:600705)
Spondyloperipheral dysplasia - short ulna (Orphanet:1856)