Narrow foot
Symptom Information:
Symptom ID: | HPO:0001786 | |||||||||||
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) Narrow foot(HPO:0001786) MedDRA: |
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Database Frequency: | 11 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
2q23.1 microdeletion syndrome | (Orphanet:228402) |
Cohen syndrome | (Orphanet:193) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Intellectual deficit, X-linked - craniofacioskeletal syndrome | (Orphanet:163979) |
Mesomelia-synostoses syndrome | (Orphanet:2496) |
Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies | (Orphanet:369897) |
Pitt-Hopkins syndrome | (Orphanet:2896) |
Prader-Willi syndrome | (Orphanet:739) |
RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION | (OMIM:268050) |
Renpenning syndrome | (Orphanet:3242) |
Van den Ende-Gupta syndrome | (Orphanet:2460) |