Hyperplasia of midface

Symptom Information:

Symptom ID: HPO:0012371
Synonyms:
Midface hyperplasia [HPO:0012371]
Midface hypertrophy [HPO:0012371]
Prominent premaxillary region/midface [Orphanet:3520]
Midface prominence [Orphanet:3520]
Quality:
Cross references:
Orphanet:3520 "Prominent premaxillary region/midface" [Orphanet:3520]
Is a (Direct Parents):
HPO         Abnormality of the midface
Orphanet Abnormal facial shape
Orphanet Prominence of the premaxilla
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 midface(HPO:0000309)
                   Hyperplasia of midface(HPO:0012371)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Aicardi syndrome (Orphanet:50)
Autosomal recessive spastic paraplegia type 20 (Orphanet:101000)
Beta-thalassemia major (Orphanet:231214)
Dislocation of the hip - dysmorphism (Orphanet:2412)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Microcephaly - cervical spine fusion anomalies (Orphanet:2522)
Oculo-reno-cerebellar syndrome (Orphanet:2715)
POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY (OMIM:611087)
Paraplegia - intellectual deficit - hyperkeratosis (Orphanet:2824)
Tricho-dento-osseous syndrome (Orphanet:3352)