Prominence of the premaxilla

Symptom Information:

Symptom ID: HPO:0010759
Synonyms:
Prominent premaxilla [HPO:0010759]
Premaxillary prominence [Orphanet:3520]
Prominent premaxilla [OMIM:Prominent premaxilla]
Prominent premaxillary region/midface [Orphanet:3520]
Midface prominence [Orphanet:3520]
Quality:
Cross references:
Orphanet:3520 "Prominent premaxillary region/midface" [Orphanet:3520]
OMIM: "Prominent premaxilla" [OMIM:Prominent premaxilla]
Is a (Direct Parents):
HPO         Abnormality of the premaxilla
Orphanet Abnormal facial shape
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 skull(HPO:0000929)
                Abnormality of facial skeleton(HPO:0011821)
                   Abnormality of the maxilla(HPO:0000326)
                      Abnormality of the premaxilla(HPO:0010758)
                         Prominence of the premaxilla(HPO:0010759)
             Abnormality of the face(HPO:0000271)
                Abnormality of the midface(HPO:0000309)
                   Abnormality of the maxilla(HPO:0000326)
                      Abnormality of the premaxilla(HPO:0010758)
                         Prominence of the premaxilla(HPO:0010759)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the skull(HPO:0000929)
                   Abnormality of facial skeleton(HPO:0011821)
                      Abnormality of the maxilla(HPO:0000326)
                         Abnormality of the premaxilla(HPO:0010758)
                            Prominence of the premaxilla(HPO:0010759)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

3MC SYNDROME 2 (OMIM:265050)
Aicardi syndrome (Orphanet:50)
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB (OMIM:614437)
Large congenital melanocytic nevus (Orphanet:626)
Marshall-Smith syndrome (Orphanet:561)