Absent foot

Symptom Information:

Symptom ID: HPO:0011301
Synonyms:
Apodia [HPO:0011301]
Congenital absence of foot [HPO:0011301]
Congenital absence of foot (disorder) [Orphanet:22180]
Absent foot (finding) [Orphanet:22180]
Acheiropodia [Orphanet:22180]
Absent foot [Orphanet:22180]
Congenital absence of foot [Orphanet:22180]
Foot absent/apodia/adactyly/acheiropodia [Orphanet:22180]
Foot agenesis [Orphanet:22180]
Congenital foot malformation [MedDRA:10062332]
Anomalies of foot, congenital, not elsewhere classified [MedDRA:10062332]
Congenital foot malformation NOS [MedDRA:10062332]
Malformation foot [MedDRA:10062332]
Malformation foot NOS [MedDRA:10062332]
Other congenital anomalies of toes [MedDRA:10062332]
Other congenital deformities of feet [MedDRA:10062332]
Other congenital deformity of feet [MedDRA:10062332]
Metatarsal agenesis [MedDRA:10062332]
Foot agenesis [MedDRA:10062332]
Tarsal coalition [MedDRA:10062332]
Absent feet [OMIM:Absent feet]
Foot adactyly [Orphanet:22180]
Quality:
Cross references:
Orphanet:22180 "Foot absent/apodia/adactyly/acheiropodia" [Orphanet:22180]
OMIM: "Absent feet" [OMIM:Absent feet]
UMLS:C0265559 "Acheiropodia" [Orphanet:22180]
UMLS:C0426910 "Absent foot" [Orphanet:22180]
UMLS:C0265624 "Congenital absence of foot" [Orphanet:22180]
Is a (Direct Parents):
MedDRA Musculoskeletal and connective tissue disorders of limbs congenital
HPO         Aplasia/Hypoplasia involving bones of the feet
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)
                      Abnormality of the foot(HPO:0001760)
                         Aplasia/Hypoplasia involving bones of the feet(HPO:0006494)
                            Absent foot(HPO:0011301)
                      Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493)
                         Aplasia/Hypoplasia involving bones of the feet(HPO:0006494)
                            Absent foot(HPO:0011301)
                   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)
                            Absent foot(HPO:0011301)
             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)
                         Absent foot(HPO:0011301)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396)
       Musculoskeletal and connective tissue disorders of limbs congenital(MedDRA:10028381)
          Absent foot(HPO:0011301)
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Acheiropodia (Orphanet:931)
Adams-Oliver syndrome (Orphanet:974)
Cloacal exstrophy (Orphanet:93929)
Fuhrmann syndrome (Orphanet:2854)