Exaggerated cupid's bow
Symptom Information:
Symptom ID: | HPO:0002263 | ||||||||||||
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) Exaggerated cupid's bow(HPO:0002263) MedDRA: |
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Database Frequency: | 15 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
14q11.2 microdeletion syndrome | (Orphanet:261120) |
8q21.11 microdeletion syndrome | (Orphanet:284160) |
Ackerman syndrome | (Orphanet:2561) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Cardiocranial syndrome, Pfeiffer type | (Orphanet:2872) |
Dysmorphism - conductive hearing loss - heart defect | (Orphanet:289553) |
Gingival fibromatosis - facial dysmorphism | (Orphanet:2025) |
Keipert syndrome | (Orphanet:2662) |
Lethal osteosclerotic bone dysplasia | (Orphanet:1832) |
Malignant hyperthermia - arthrogryposis - torticollis | (Orphanet:2215) |
PALANT CLEFT PALATE SYNDROME | (OMIM:260150) |
Peters-plus syndrome | (Orphanet:709) |
Pitt-Hopkins syndrome | (Orphanet:2896) |
Wiedemann-Steiner syndrome | (Orphanet:319182) |