U-Shaped upper lip vermilion

Symptom Information:

Symptom ID: HPO:0010806
Synonyms:
Carp-like mouth [HPO:0010806]
Carp-shaped mouth [HPO:0010806]
Large, carp-shaped mouth [HPO:0010806]
Wide, carp-shaped mouth [HPO:0010806]
Carp-like mouth [OMIM:Carp-like mouth]
Carp-shaped mouth [OMIM:Carp-shaped mouth]
Large, carp-shaped mouth [OMIM:Large, carp-shaped mouth]
Wide, carp-shaped mouth [OMIM:Wide, carp-shaped mouth]
'Carp-like' mouth [OMIM:'Carp-like' mouth]
Quality:
Cross references:
OMIM: "Carp-like mouth" [OMIM:Carp-like mouth]
OMIM: "Carp-shaped mouth" [OMIM:Carp-shaped mouth]
OMIM: "Large, carp-shaped mouth" [OMIM:Large, carp-shaped mouth]
OMIM: "Wide, carp-shaped mouth" [OMIM:Wide, carp-shaped mouth]
OMIM: "'Carp-like' mouth" [OMIM:'Carp-like' mouth]
Is a (Direct Parents):
HPO         Abnormality of upper lip vermillion
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:
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)