Split foot

Symptom Information:

Symptom ID: HPO:0001839
Synonyms:
Ectrodactyly (feet) [HPO:0001839]
Lobster-claw foot deformity [HPO:0001839]
Split-foot [HPO:0001839]
Split foot (disorder) [Orphanet:22160]
Split foot [Orphanet:22160]
Lobster-claw foot deformity [OMIM:Lobster-claw foot deformity]
Split foot [OMIM:Split foot]
Split-foot [OMIM:Split-foot]
Median ray abnormal/split foot [Orphanet:22160]
Quality:
Cross references:
Orphanet:22160 "Median ray abnormal/split foot" [Orphanet:22160]
OMIM: "Lobster-claw foot deformity" [OMIM:Lobster-claw foot deformity]
OMIM: "Split foot" [OMIM:Split foot]
OMIM: "Split-foot" [OMIM:Split-foot]
UMLS:C0432028 "Split foot" [Orphanet:22160]
Is a (Direct Parents):
Orphanet Abnormality of the foot
HPO         Ectrodactyly
HPO         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)
                         Split foot(HPO:0001839)
                   Ectrodactyly(HPO:0100257)
                      Split foot(HPO:0001839)
MedDRA:
Database Frequency: 28 / 7739
Resource:

All diseases associated with this symptom:

ACRORENAL SYNDROME, AUTOSOMAL RECESSIVE (OMIM:201310)
ADULT syndrome (Orphanet:978)
Acro-cardio-facial syndrome (Orphanet:2008)
Acro-renal-mandibular syndrome (Orphanet:958)
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
Distal limb deficiencies - micrognathia syndrome (Orphanet:1307)
ECTRODACTYLY AND ECTODERMAL DYSPLASIA WITHOUT CLEFT LIP/PALATE (OMIM:129810)
ECTRODACTYLY OF LOWER LIMBS, CONGENITAL HEART DEFECT, AND MICROGNATHIA (OMIM:601348)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
Ectrodactyly - polydactyly (Orphanet:1892)
Fibular aplasia - ectrodactyly (Orphanet:1118)
Focal dermal hypoplasia (Orphanet:2092)
Karsch-Neugebauer syndrome (Orphanet:2329)
Limb-mammary syndrome (Orphanet:69085)
MMEP syndrome (Orphanet:3434)
Patterson-Stevenson-Fontaine syndrome (Orphanet:2439)
SPLIT-HAND AND SPLIT-FOOT WITH HYPODONTIA (OMIM:183500)
SPLIT-HAND/FOOT MALFORMATION 1 (OMIM:183600)
SPLIT-HAND/FOOT MALFORMATION 2 (OMIM:313350)
SPLIT-HAND/FOOT MALFORMATION 6 (OMIM:225300)
Split hand - split foot - deafness (Orphanet:71271)
Split hand - urinary anomalies - spina bifida (Orphanet:2437)
Split hand-split foot malformation (Orphanet:2440)
Tetramelic monodactyly (Orphanet:2564)
Tibial aplasia - ectrodactyly (Orphanet:3329)
Triphalangeal thumbs - brachyectrodactyly (Orphanet:2947)
Ulnar hypoplasia - split foot (Orphanet:1122)