Narrow nasal bridge

Symptom Information:

Symptom ID: HPO:0000446
Synonyms:
Nasal bridge, thin [HPO:0000446]
Narrow nasal root [HPO:0000446]
Nasal Bridge, Narrow [HPO:0000446]
Pinched nasal bridge [HPO:0000446]
Narrow nasal root [Orphanet:8420]
Narrow nose (finding) [Orphanet:8120]
Narrow nasal bridge [OMIM:Narrow nasal bridge]
Narrow nasal bridge [Orphanet:8120]
Narrow nasal bridge (12 of 22) [OMIM:Narrow nasal bridge (12 of 22)]
Quality:
Cross references:
HPO:0000418 "Narrow nasal ridge" [Orphanet:8120]
Orphanet:8420 "Narrow nasal root" [Orphanet:8420]
Orphanet:8120 "Narrow nasal bridge" [Orphanet:8120]
OMIM: "Narrow nasal bridge" [OMIM:Narrow nasal bridge]
OMIM: "Narrow nasal bridge (12 of 22)" [OMIM:Narrow nasal bridge (12 of 22)]
Is a (Direct Parents):
HPO         Abnormality of the nasal bridge
Orphanet Abnormality of the nose
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 nose(HPO:0000366)
                   Abnormality of the nasal bridge(HPO:0000422)
                      Narrow nasal bridge(HPO:0000446)
MedDRA:
Database Frequency: 29 / 7739
Resource:

All diseases associated with this symptom:

19p13.12 microdeletion syndrome (Orphanet:254346)
Baller-Gerold syndrome (Orphanet:1225)
Conductive deafness - ptosis - skeletal anomalies (Orphanet:3236)
Dysostosis, Stanescu type (Orphanet:1798)
Ectodermal dysplasia - blindness (Orphanet:1806)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Fibular aplasia - complex brachydactyly (Orphanet:2639)
Focal dermal hypoplasia (Orphanet:2092)
Fryns-Smeets-Thiry syndrome (Orphanet:2058)
Intellectual deficit - dysmorphism - hypogonadism - diabetes mellitus (Orphanet:3044)
Intellectual deficit - polydactyly - uncombable hair (Orphanet:3082)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
Kenny-Caffey syndrome (Orphanet:2333)
LUJAN-FRYNS SYNDROME (OMIM:309520)
Microbrachycephaly - ptosis - cleft lip (Orphanet:2511)
Microcephalic osteodysplastic dysplasia, Saul-Wilson type (Orphanet:85172)
Norrie disease (Orphanet:649)
OCULODENTODIGITAL DYSPLASIA (OMIM:164200)
Oculodentodigital dysplasia (Orphanet:2710)
Prader-Willi syndrome (Orphanet:739)
Pseudoprogeria syndrome (Orphanet:2985)
RAPADILINO syndrome (Orphanet:3021)
Solitary median maxillary central incisor syndrome (Orphanet:2286)
Stoll-Alembik-Finck syndrome (Orphanet:3200)
Torg-Winchester syndrome (Orphanet:3460)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Trichodental syndrome (Orphanet:3351)
Van den Ende-Gupta syndrome (Orphanet:2460)
Waardenburg syndrome type 3 (Orphanet:896)