Exaggerated cupid's bow

Symptom Information:

Symptom ID: HPO:0002263
Cupid bow upper lip [HPO:0002263]
Cupid-bow shaped upper lip [HPO:0002263]
Prominent cupid-bow of upper lip [HPO:0002263]
Synonym: Cupid's bow, accentuated [HPO:0002263]
Exaggerated Cupid's bow [Orphanet:9400]
Cupid bow upper lip [OMIM:Cupid bow upper lip]
Cupid-bow shaped upper lip [OMIM:Cupid-bow shaped upper lip]
Prominent cupid-bow of upper lip [OMIM:Prominent cupid-bow of upper lip]
Exaggerated cupid bows [Orphanet:9400]
Cupid bow shaped upper lip [OMIM:Cupid bow shaped upper lip]
Cupid's bow upper lip [OMIM:Cupid's bow upper lip]
Cupid's bow, exaggerated (in some patients) [OMIM:Cupid's bow, exaggerated (in some patients)]
Cross references:
Orphanet:9400 "Exaggerated cupid bows" [Orphanet:9400]
OMIM: "Cupid bow upper lip" [OMIM:Cupid bow upper lip]
OMIM: "Cupid-bow shaped upper lip" [OMIM:Cupid-bow shaped upper lip]
OMIM: "Prominent cupid-bow of upper lip" [OMIM:Prominent cupid-bow of upper lip]
OMIM: "Cupid bow shaped upper lip" [OMIM:Cupid bow shaped upper lip]
OMIM: "Cupid's bow upper lip" [OMIM:Cupid's bow upper lip]
OMIM: "Cupid's bow, exaggerated (in some patients)" [OMIM:Cupid's bow, exaggerated (in some patients)]
Is a (Direct Parents):
Orphanet Abnormality of the mouth
HPO         Abnormality of upper lip vermillion
Is a (Whole tree): HPO:
    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)
Database Frequency: 15 / 7739

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)
Peters-plus syndrome (Orphanet:709)
Pitt-Hopkins syndrome (Orphanet:2896)
Wiedemann-Steiner syndrome (Orphanet:319182)