Broad foot
Symptom Information:
Symptom ID: | HPO:0001769 | ||||
Synonyms: |
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Quality: | |||||
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 the lower limb(HPO:0002814) Abnormality of the foot(HPO:0001760) Broad foot(HPO:0001769) MedDRA: |
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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) |