Short hallux

Symptom Information:

Symptom ID: HPO:0010109
Synonyms:
Hypoplastic big toes [HPO:0010109]
Hypoplastic hallux [HPO:0010109]
Short halluces [HPO:0010109]
Small hallux [HPO:0010109]
Hypoplastic big toes [OMIM:Hypoplastic big toes]
Short halluces [OMIM:Short halluces]
Short hallux [OMIM:Short hallux]
Short big toe [Orphanet:22520]
Quality:
Cross references:
Orphanet:22520 "Short big toe" [Orphanet:22520]
OMIM: "Hypoplastic big toes" [OMIM:Hypoplastic big toes]
OMIM: "Short halluces" [OMIM:Short halluces]
OMIM: "Short hallux" [OMIM:Short hallux]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of the hallux
Orphanet Abnormality of the hallux
HPO         Short toe
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 digit(HPO:0011297)
                      Short digit(HPO:0011927)
                         Short toe(HPO:0001831)
                            Short hallux(HPO:0010109)
                      Abnormality of toe(HPO:0001780)
                         Aplasia/Hypoplasia of toe(HPO:0001991)
                            Short toe(HPO:0001831)
                               Short hallux(HPO:0010109)
                            Absent toe(HPO:0010760)
                               Aplasia/Hypoplasia of the hallux(HPO:0008362)
                                  Short hallux(HPO:0010109)
                         Abnormality of the hallux(HPO:0001844)
                            Aplasia/Hypoplasia of the hallux(HPO:0008362)
                               Short hallux(HPO:0010109)
                   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 toe(HPO:0001991)
                               Short toe(HPO:0001831)
                                  Short hallux(HPO:0010109)
                               Absent toe(HPO:0010760)
                                  Aplasia/Hypoplasia of the hallux(HPO:0008362)
                                     Short hallux(HPO:0010109)
                   Abnormality of the lower limb(HPO:0002814)
                      Abnormality of the foot(HPO:0001760)
                         Abnormality of toe(HPO:0001780)
                            Aplasia/Hypoplasia of toe(HPO:0001991)
                               Short toe(HPO:0001831)
                                  Short hallux(HPO:0010109)
                               Absent toe(HPO:0010760)
                                  Aplasia/Hypoplasia of the hallux(HPO:0008362)
                                     Short hallux(HPO:0010109)
                            Abnormality of the hallux(HPO:0001844)
                               Aplasia/Hypoplasia of the hallux(HPO:0008362)
                                  Short hallux(HPO:0010109)
                         Aplasia/Hypoplasia involving bones of the feet(HPO:0006494)
                            Aplasia/Hypoplasia of toe(HPO:0001991)
                               Short toe(HPO:0001831)
                                  Short hallux(HPO:0010109)
                               Absent toe(HPO:0010760)
                                  Aplasia/Hypoplasia of the hallux(HPO:0008362)
                                     Short hallux(HPO:0010109)
                      Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493)
                         Aplasia/Hypoplasia involving bones of the feet(HPO:0006494)
                            Aplasia/Hypoplasia of toe(HPO:0001991)
                               Short toe(HPO:0001831)
                                  Short hallux(HPO:0010109)
                               Absent toe(HPO:0010760)
                                  Aplasia/Hypoplasia of the hallux(HPO:0008362)
                                     Short hallux(HPO:0010109)
             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 toe(HPO:0001991)
                            Short toe(HPO:0001831)
                               Short hallux(HPO:0010109)
                            Absent toe(HPO:0010760)
                               Aplasia/Hypoplasia of the hallux(HPO:0008362)
                                  Short hallux(HPO:0010109)
MedDRA:
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

Acro-renal-ocular syndrome (Orphanet:959)
Brachydactyly - preaxial hallux varus (Orphanet:1278)
Brachydactyly type A1 (Orphanet:93388)
Brachydactyly type A2 (Orphanet:93396)
Cleft palate - stapes fixation - oligodontia (Orphanet:2010)
Deafness - genital anomalies - metacarpal and metatarsal synostosis (Orphanet:3224)
Fibrodysplasia ossificans progressiva (Orphanet:337)
Guttmacher syndrome (Orphanet:2957)
Hand-foot-genital syndrome (Orphanet:2438)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Keipert syndrome (Orphanet:2662)
Keutel syndrome (Orphanet:85202)
MULTIPLE SYNOSTOSES SYNDROME 1 (OMIM:186500)
Mesoaxial synostotic syndactyly with phalangeal reduction (Orphanet:157801)
Mononen-Karnes-Senac syndrome (Orphanet:2565)
Multiple synostoses syndrome (Orphanet:3237)
OTOFACIOOSSEOUS-GONADAL SYNDROME (OMIM:601976)
Oculodentodigital dysplasia (Orphanet:2710)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 1 (Orphanet:90650)
Otopalatodigital syndrome type 2 (Orphanet:90652)
Pfeiffer syndrome type 1 (Orphanet:93258)
Pfeiffer syndrome type 2 (Orphanet:93259)
Pfeiffer syndrome type 3 (Orphanet:93260)
SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 1 (OMIM:119100)
Tibial aplasia - ectrodactyly (Orphanet:3329)
Wolf-Hirschhorn syndrome (Orphanet:280)