Long foot

Symptom Information:

Symptom ID: HPO:0001833
Synonyms:
Disproportionately large feet [HPO:0001833]
long feet [HPO:0001833]
Broad foot [Orphanet:22060]
Disproportionately large feet [OMIM:Disproportionately large feet]
Long feet [OMIM:Long feet]
Long foot/arachnodactyly of toes [Orphanet:22020]
Long foot [Orphanet:22020]
Long foot (finding) [Orphanet:22020]
Quality:
Cross references:
HPO:0001769 "Broad foot" [Orphanet:22060]
Orphanet:22060 "Broad foot" [Orphanet:22060]
Orphanet:22020 "Long foot/arachnodactyly of toes" [Orphanet:22020]
OMIM: "Disproportionately large feet" [OMIM:Disproportionately large feet]
OMIM: "Long feet" [OMIM:Long feet]
UMLS:C0576225 "Long foot" [Orphanet:22020]
Is a (Direct Parents):
HPO         Abnormality of the foot
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)
                         Long foot(HPO:0001833)
MedDRA:
Database Frequency: 33 / 7739
Resource:

All diseases associated with this symptom:

17q11.2 microduplication syndrome (Orphanet:139474)
17q23.1q23.2 microdeletion syndrome (Orphanet:261279)
5p13 microduplication syndrome (Orphanet:329802)
ASPARAGINE SYNTHETASE DEFICIENCY (OMIM:615574)
Arachnodactyly - intellectual deficit - dysmorphism (Orphanet:1130)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
CHROMOSOME Xq26.3 DUPLICATION SYNDROME (OMIM:300942)
COCKAYNE SYNDROME, TYPE III (OMIM:216411)
Cohen syndrome (Orphanet:193)
DERMATOLEUKODYSTROPHY (OMIM:221790)
Distal monosomy 19p13.3 (Orphanet:96129)
Frontometaphyseal dysplasia (Orphanet:1826)
GIACHETI SYNDROME (OMIM:612917)
Intellectual deficit, X-linked, Stevenson type (Orphanet:85325)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 (OMIM:608594)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 (OMIM:269700)
Leprechaunism (Orphanet:508)
MENTAL RETARDATION, X-LINKED 19 (OMIM:300844)
MENTAL RETARDATION, X-LINKED, SYNDROMIC 14 (OMIM:300676)
MOMO syndrome (Orphanet:2563)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Oculocerebrofacial syndrome, Kaufman type (Orphanet:2707)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Pseudoleprechaunism syndrome, Patterson type (Orphanet:2976)
Schilbach-Rott syndrome (Orphanet:2353)
Sotos syndrome (Orphanet:821)
Trisomy 1q (Orphanet:261344)
Van den Ende-Gupta syndrome (Orphanet:2460)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
X-linked intellectual deficit with marfanoid habitus (Orphanet:776)
Zechi-Ceide syndrome (Orphanet:217017)
Zunich-Kaye syndrome (Orphanet:3474)