Broad philtrum

Symptom Information:

Symptom ID: HPO:0000289
Synonyms:
Wide philtrum [HPO:0000289]
Broad philtrum [OMIM:Broad philtrum]
Wide philtrum [OMIM:Wide philtrum]
Philtrum flat/large/featureless/absent cupidon bows [Orphanet:9640]
Quality:
Cross references:
Orphanet:9640 "Philtrum flat/large/featureless/absent cupidon bows" [Orphanet:9640]
OMIM: "Broad philtrum" [OMIM:Broad philtrum]
OMIM: "Wide philtrum" [OMIM:Wide philtrum]
Is a (Direct Parents):
Orphanet Abnormality of the mouth
HPO         Abnormality of the philtrum
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 philtrum(HPO:0000288)
                      Broad philtrum(HPO:0000289)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

3MC SYNDROME 2 (OMIM:265050)
AARSKOG-SCOTT SYNDROME (OMIM:305400)
AREDYLD syndrome (Orphanet:1133)
Ackerman syndrome (Orphanet:2561)
CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKEFACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION (OMIM:601088)
Cerebro-oculo-nasal syndrome (Orphanet:66625)
Costello syndrome (Orphanet:3071)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY (OMIM:602342)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES (OMIM:600093)
THAI SYMPHALANGISM SYNDROME (OMIM:608028)