Thick upper lip vermilion

Symptom Information:

Symptom ID: HPO:0000215
Synonyms:
Prominent upper lip [HPO:0000215]
Thick upper lip [HPO:0000215]
Thick vermilion border of upper lip [HPO:0000215]
Thick upper lip vermillon [Orphanet:9120]
Prominent upper lip [OMIM:Prominent upper lip]
Thick lips [Orphanet:9120]
Thick lips (in males) [OMIM:Thick lips (in males)]
Quality:
Cross references:
Orphanet:9120 "Thick lips" [Orphanet:9120]
OMIM: "Prominent upper lip" [OMIM:Prominent upper lip]
OMIM: "Thick lips (in males)" [OMIM:Thick lips (in males)]
Is a (Direct Parents):
HPO         Thick vermilion border
Orphanet Abnormality of the mouth
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)
                            Thick upper lip vermilion(HPO:0000215)
                      Thick vermilion border(HPO:0012471)
                         Thick upper lip vermilion(HPO:0000215)
MedDRA:
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

48,XXYY syndrome (Orphanet:10)
Costello syndrome (Orphanet:3071)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Intellectual deficit, X-linked, Wilson type (Orphanet:85290)
Keipert syndrome (Orphanet:2662)
Late-onset localized junctional epidermolysis bullosa - intellectual deficit (Orphanet:231556)
Lathosterolosis (Orphanet:46059)
Leprechaunism (Orphanet:508)
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III (OMIM:210730)
Marshall syndrome (Orphanet:560)
Miller-Dieker syndrome (Orphanet:531)
Multiple synostoses syndrome (Orphanet:3237)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY (OMIM:611087)
Premature ageing appearance-developmental delay-cardiac arrhythmia syndrome (Orphanet:276432)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES (OMIM:600093)
Spondyloepiphyseal dysplasia, Cantu type (Orphanet:163654)