Oval face
Symptom Information:
Symptom ID: | HPO:0000300 | ||
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 head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Abnormal facial shape(HPO:0001999) Oval face(HPO:0000300) MedDRA: |
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Database Frequency: | 5 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
Congenital lethal myopathy, Compton-North type | (Orphanet:210163) |
Glomerulonephritis - sparse hair - telangiectasis | (Orphanet:2087) |
Spondyloepimetaphyseal dysplasia with joint laxity | (Orphanet:93359) |
X-linked intellectual deficit, Najm type | (Orphanet:163937) |