U-Shaped upper lip vermilion
Symptom Information:
Symptom ID: | HPO:0010806 | |||||||||
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 head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Abnormality of the mouth(HPO:0000153) Abnormality of the lip(HPO:0000159) Abnormality of upper lip(HPO:0000177) Abnormality of upper lip vermillion(HPO:0011339) U-Shaped upper lip vermilion(HPO:0010806) MedDRA: |
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Database Frequency: | 18 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
Acromelic frontonasal dysplasia | (Orphanet:1827) |
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA | (OMIM:609945) |
Carpenter-Waziri syndrome | (Orphanet:93973) |
Cerebro-oculo-nasal syndrome | (Orphanet:66625) |
Chudley-Lowry-Hoar syndrome | (Orphanet:93971) |
Hall-Riggs syndrome | (Orphanet:2107) |
Holmes-Gang syndrome | (Orphanet:93970) |
Intellectual disability-developmental delay-contractures syndrome | (Orphanet:3454) |
Jacobsen syndrome | (Orphanet:2308) |
Juberg-Marsidi syndrome | (Orphanet:93972) |
Kleefstra syndrome | (Orphanet:261494) |
Microcephaly - facio-cardio-skeletal syndrome, Hadziselimovic type | (Orphanet:217026) |
Monosomy 18q | (Orphanet:1600) |
Renier-Gabreels-Jasper syndrome | (Orphanet:93975) |
Simpson-Golabi-Behmel syndrome type 2 | (Orphanet:79022) |
Smith-Fineman-Myers syndrome | (Orphanet:93974) |
X-linked intellectual deficit - hypotonic face | (Orphanet:73220) |