Foot oligodactyly

Symptom Information:

Symptom ID: HPO:0001849
Synonyms:
Missing toes [HPO:0001849]
Oligodactyly of feet [HPO:0001849]
Missing toes [OMIM:Missing toes]
Oligodactyly (45%) [OMIM:Oligodactyly (45%)]
Quality:
Cross references:
OMIM: "Missing toes" [OMIM:Missing toes]
OMIM: "Oligodactyly (45%)" [OMIM:Oligodactyly (45%)]
Is a (Direct Parents):
HPO         Oligodactyly
HPO         Absent 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)
                      Abnormality of toe(HPO:0001780)
                         Aplasia/Hypoplasia of toe(HPO:0001991)
                            Absent toe(HPO:0010760)
                               Foot oligodactyly(HPO:0001849)
                      Oligodactyly(HPO:0012165)
                         Foot oligodactyly(HPO:0001849)
                   Abnormality of the lower limb(HPO:0002814)
                      Abnormality of the foot(HPO:0001760)
                         Aplasia/Hypoplasia involving bones of the feet(HPO:0006494)
                            Aplasia/Hypoplasia of toe(HPO:0001991)
                               Absent toe(HPO:0010760)
                                  Foot oligodactyly(HPO:0001849)
                         Abnormality of toe(HPO:0001780)
                            Aplasia/Hypoplasia of toe(HPO:0001991)
                               Absent toe(HPO:0010760)
                                  Foot oligodactyly(HPO:0001849)
                      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)
                               Absent toe(HPO:0010760)
                                  Foot oligodactyly(HPO:0001849)
                   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)
                               Absent toe(HPO:0010760)
                                  Foot oligodactyly(HPO:0001849)
             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)
                            Absent toe(HPO:0010760)
                               Foot oligodactyly(HPO:0001849)
MedDRA:
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY (OMIM:601357)
FIBULAR APLASIA, TIBIAL CAMPOMELIA, AND OLIGOSYNDACTYLY SYNDROME (OMIM:246570)
Focal dermal hypoplasia (Orphanet:2092)
Fuhrmann syndrome (Orphanet:2854)
Microphthalmia with limb anomalies (Orphanet:1106)
Nager syndrome (Orphanet:245)
Phocomelia, Schinzel type (Orphanet:2879)
SPLIT-HAND/FOOT MALFORMATION 6 (OMIM:225300)
Split hand-split foot malformation (Orphanet:2440)