Foot monodactyly

Symptom Information:

Symptom ID: HPO:0200054
Synonyms:
Monodactyly [OMIM:Monodactyly]
Monodactyly (some) [OMIM:Monodactyly (some)]
Quality:
Cross references:
OMIM: "Monodactyly" [OMIM:Monodactyly]
OMIM: "Monodactyly (some)" [OMIM:Monodactyly (some)]
Is a (Direct Parents):
HPO         Foot oligodactyly
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)
                                  Foot monodactyly(HPO:0200054)
                      Oligodactyly(HPO:0012165)
                         Foot oligodactyly(HPO:0001849)
                            Foot monodactyly(HPO:0200054)
                   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)
                                     Foot monodactyly(HPO:0200054)
                         Abnormality of toe(HPO:0001780)
                            Aplasia/Hypoplasia of toe(HPO:0001991)
                               Absent toe(HPO:0010760)
                                  Foot oligodactyly(HPO:0001849)
                                     Foot monodactyly(HPO:0200054)
                      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)
                                     Foot monodactyly(HPO:0200054)
                   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)
                                     Foot monodactyly(HPO:0200054)
             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)
                                  Foot monodactyly(HPO:0200054)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

CHARGE syndrome (Orphanet:138)
CHROMOSOME 17p13.3, TELOMERIC, DUPLICATION SYNDROME (OMIM:612576)
Gollop-Wolfgang complex (Orphanet:1986)
Karsch-Neugebauer syndrome (Orphanet:2329)
SPLIT-HAND/FOOT MALFORMATION 1 (OMIM:183600)
Tetramelic monodactyly (Orphanet:2564)