Broad foot

Symptom Information:

Symptom ID: HPO:0001769
Synonyms:
Broad feet [HPO:0001769]
Broad feet [OMIM:Broad feet]
Broad foot [Orphanet:22060]
Quality:
Cross references:
HPO:0001833 "Large feet" [Orphanet:22060]
Orphanet:22060 "Broad foot" [Orphanet:22060]
OMIM: "Broad feet" [OMIM:Broad feet]
Is a (Direct Parents):
Orphanet Abnormality of the foot
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)
                         Broad foot(HPO:0001769)
MedDRA:
Database Frequency: 31 / 7739
Resource:

All diseases associated with this symptom:

3MC SYNDROME 1 (OMIM:257920)
AARSKOG-SCOTT SYNDROME (OMIM:305400)
Aarskog-Scott syndrome (Orphanet:915)
Acromegaly (Orphanet:963)
Alström syndrome (Orphanet:64)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Borjeson-Forssman-Lehmann syndrome (Orphanet:127)
CHONDRODYSPLASIA, ACROMESOMELIC, WITH GENITAL ANOMALIES (OMIM:609441)
DESBUQUOIS DYSPLASIA 2 (OMIM:615777)
DYGGVE-MELCHIOR-CLAUSEN DISEASE (OMIM:223800)
Dermatoosteolysis, Kirghizian type (Orphanet:1657)
Dyggve-Melchior-Clausen disease (Orphanet:239)
Gonadal dysgenesis, XY type - associated anomalies (Orphanet:1770)
HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVEFACIAL FEATURES (OMIM:609943)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 (OMIM:608594)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 (OMIM:269700)
Laurin-Sandrow syndrome (Orphanet:2378)
Leprechaunism (Orphanet:508)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
Muckle-Wells syndrome (Orphanet:575)
Neu-Laxova syndrome (Orphanet:2671)
Osteoglophonic dwarfism (Orphanet:2645)
PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY (OMIM:602342)
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism (Orphanet:3085)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Sillence syndrome (Orphanet:3168)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Spondyloepimetaphyseal dysplasia, Bieganski type (Orphanet:168448)
Spondyloepimetaphyseal dysplasia, Irapa type (Orphanet:93351)
Tetrasomy 12p (Orphanet:884)
Weaver syndrome (Orphanet:3447)