Sandal gap

Symptom Information:

Symptom ID: HPO:0001852
Synonyms:
Gap between 1st and 2nd toes [HPO:0001852]
Gap between first and second toe [HPO:0001852]
Increased space between first and second toes [HPO:0001852]
Sandal gap between first and second toes [HPO:0001852]
Space between great toe and second toe [HPO:0001852]
Wide space between 1st, 2nd ties [HPO:0001852]
Wide space between first and second toes [HPO:0001852]
Widely spaced 1st-2nd toes [HPO:0001852]
Widely spaced first and second toes [HPO:0001852]
Widened gap 1st-2nd toes [HPO:0001852]
Widened gap first and second toe [HPO:0001852]
Gap between 1st and 2nd toes [OMIM:Gap between 1st and 2nd toes]
Gap between first and second toe [OMIM:Gap between first and second toe]
Increased space between first and second toes [OMIM:Increased space between first and second toes]
Sandal gap [OMIM:Sandal gap]
Sandal gap between first and second toes [OMIM:Sandal gap between first and second toes]
Space between great toe and second toe [OMIM:Space between great toe and second toe]
Wide space between 1st, 2nd ties [OMIM:Wide space between 1st, 2nd ties]
Wide space between first and second toes [OMIM:Wide space between first and second toes]
Widely spaced 1st-2nd toes [OMIM:Widely spaced 1st-2nd toes]
Widely spaced first and second toes [OMIM:Widely spaced first and second toes]
Widened gap 1st-2nd toes [OMIM:Widened gap 1st-2nd toes]
Widened gap first and second toe [OMIM:Widened gap first and second toe]
Wide space between 1st-2nd toes [Orphanet:22620]
'Sandal gap' between first and second toes [OMIM:'Sandal gap' between first and second toes]
Gap between first and second toes [OMIM:Gap between first and second toes]
Sandal gap (1/4 patients) [OMIM:Sandal gap (1/4 patients)]
Sandal gap (in one family) [OMIM:Sandal gap (in one family)]
Widely spaced first and second toe [OMIM:Widely spaced first and second toe]
Quality:
Cross references:
Orphanet:22620 "Wide space between 1st-2nd toes" [Orphanet:22620]
OMIM: "Gap between 1st and 2nd toes" [OMIM:Gap between 1st and 2nd toes]
OMIM: "Gap between first and second toe" [OMIM:Gap between first and second toe]
OMIM: "Increased space between first and second toes" [OMIM:Increased space between first and second toes]
OMIM: "Sandal gap" [OMIM:Sandal gap]
OMIM: "Sandal gap between first and second toes" [OMIM:Sandal gap between first and second toes]
OMIM: "Space between great toe and second toe" [OMIM:Space between great toe and second toe]
OMIM: "Wide space between 1st, 2nd ties" [OMIM:Wide space between 1st, 2nd ties]
OMIM: "Wide space between first and second toes" [OMIM:Wide space between first and second toes]
OMIM: "Widely spaced 1st-2nd toes" [OMIM:Widely spaced 1st-2nd toes]
OMIM: "Widely spaced first and second toes" [OMIM:Widely spaced first and second toes]
OMIM: "Widened gap 1st-2nd toes" [OMIM:Widened gap 1st-2nd toes]
OMIM: "Widened gap first and second toe" [OMIM:Widened gap first and second toe]
OMIM: "'Sandal gap' between first and second toes" [OMIM:'Sandal gap' between first and second toes]
OMIM: "Gap between first and second toes" [OMIM:Gap between first and second toes]
OMIM: "Sandal gap (1/4 patients)" [OMIM:Sandal gap (1/4 patients)]
OMIM: "Sandal gap (in one family)" [OMIM:Sandal gap (in one family)]
OMIM: "Widely spaced first and second toe" [OMIM:Widely spaced first and second toe]
Is a (Direct Parents):
Orphanet Abnormality of the foot
HPO         Abnormality of toe
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)
                         Sandal gap(HPO:0001852)
                   Abnormality of the lower limb(HPO:0002814)
                      Abnormality of the foot(HPO:0001760)
                         Abnormality of toe(HPO:0001780)
                            Sandal gap(HPO:0001852)
MedDRA:
Database Frequency: 63 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
17q21.31 microduplication syndrome (Orphanet:217340)
17q23.1q23.2 microdeletion syndrome (Orphanet:261279)
19p13.12 microdeletion syndrome (Orphanet:254346)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
2q23.1 microdeletion syndrome (Orphanet:228402)
2q31.1 microdeletion syndrome (Orphanet:251014)
3q29 microduplication (Orphanet:251038)
8q22.1 microdeletion syndrome (Orphanet:178303)
APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIALDYSMORPHISM, AND OTHER CONGENITAL ANOMALIES (OMIM:300887)
Acro-oto-ocular syndrome (Orphanet:2980)
Acro-renal-ocular syndrome (Orphanet:959)
Atelosteogenesis type II (Orphanet:56304)
Atelosteogenesis type III (Orphanet:56305)
Autosomal dominant nonsyndromic intellectual deficit (Orphanet:178469)
Autosomal recessive Robinow syndrome (Orphanet:1507)
CARDIAC MALFORMATION, CLEFT LIP/PALATE, MICROCEPHALY AND DIGITAL ANOMALIES (OMIM:600987)
CLOVE syndrome (Orphanet:140944)
Cabezas syndrome (Orphanet:85293)
Cleft palate - stapes fixation - oligodontia (Orphanet:2010)
Cohen syndrome (Orphanet:193)
Coxo-podo-patellar syndrome (Orphanet:1509)
Craniofrontonasal dysplasia (Orphanet:1520)
Craniomicromelic syndrome (Orphanet:1524)
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies (Orphanet:221145)
DESBUQUOIS DYSPLASIA 1 (OMIM:251450)
Desbuquois syndrome (Orphanet:1425)
Developmental delay with autism spectrum disorder and gait instability (Orphanet:329195)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Down syndrome (Orphanet:870)
Dubowitz syndrome (Orphanet:235)
Ectodermal dysplasia - intellectual deficit - central nervous system malformation (Orphanet:1812)
Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria (Orphanet:1035)
Endocrine-cerebro-osteodysplasia syndrome (Orphanet:199332)
Endomyocardial fibroelastosis (Orphanet:2022)
Eye defects - arachnodactyly - cardiopathy (Orphanet:2725)
Greenberg dysplasia (Orphanet:1426)
Hallux varus - preaxial polysyndactyly (Orphanet:2110)
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly (Orphanet:2180)
Intellectual deficit - balding - patella luxation - acromicria (Orphanet:3041)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
Kapur-Toriello syndrome (Orphanet:2328)
Kousseff syndrome (Orphanet:2351)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
Lethal acantholytic epidermolysis bullosa (Orphanet:158687)
Lethal faciocardiomelic dysplasia (Orphanet:1972)
Lethal hemolytic anemia - genital anomalies (Orphanet:1046)
Microcephaly-cardiomyopathy syndrome (Orphanet:2515)
Microphthalmia with limb anomalies (Orphanet:1106)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Oculo-reno-cerebellar syndrome (Orphanet:2715)
Okihiro syndrome (Orphanet:93293)
Otopalatodigital syndrome type 1 (Orphanet:90650)
Pierre Robin syndrome - faciodigital anomaly (Orphanet:2888)
Ring chromosome 10 (Orphanet:1438)
Roberts syndrome (Orphanet:3103)
SECKEL SYNDROME 1 (OMIM:210600)
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY (OMIM:614800)
Seckel syndrome (Orphanet:808)
Syndactyly type 2 (Orphanet:93403)
TOES, SPACE BETWEEN FIRST AND SECOND (OMIM:189230)
Toriello-Carey syndrome (Orphanet:3338)
Weaver syndrome (Orphanet:3447)