Sandal gap
Symptom Information:
Symptom ID: | HPO:0001852 | |||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |