Narrow foot

Symptom Information:

Symptom ID: HPO:0001786
Synonyms:
Slender feet [HPO:0001786]
Narrow foot (finding) [Orphanet:22140]
Small foot (finding) [Orphanet:22140]
Narrow foot [Orphanet:22140]
Small foot [Orphanet:22140]
Slender feet [OMIM:Slender feet]
Narrow feet [OMIM:Narrow feet]
Small feet (<10th percentile for height age) [OMIM:Small feet (<10th percentile for height age)]
Small feet (deletion patients) [OMIM:Small feet (deletion patients)]
Small feet (in some patients) [OMIM:Small feet (in some patients)]
Small feet (male and female) [OMIM:Small feet (male and female)]
Quality:
Cross references:
Orphanet:22140 "Small foot" [Orphanet:22140]
OMIM: "Slender feet" [OMIM:Slender feet]
OMIM: "Narrow feet" [OMIM:Narrow feet]
OMIM: "Small feet (<10th percentile for height age)" [OMIM:Small feet (<10th percentile for height age)]
OMIM: "Small feet (deletion patients)" [OMIM:Small feet (deletion patients)]
OMIM: "Small feet (in some patients)" [OMIM:Small feet (in some patients)]
OMIM: "Small feet (male and female)" [OMIM:Small feet (male and female)]
UMLS:C0576227 "Narrow foot" [Orphanet:22140]
UMLS:C0576224 "Small foot" [Orphanet:22140]
Is a (Direct Parents):
Orphanet Abnormality of the foot
HPO         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)
                         Narrow foot(HPO:0001786)
MedDRA:
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)