Narrow nasal ridge

Symptom Information:

Symptom ID: HPO:0000418
Synonyms:
Pinched nose [HPO:0000418]
Narrow nasal bridge [Orphanet:8120]
Narrow nose (finding) [Orphanet:8120]
Pinched nose [OMIM:Pinched nose]
Narrow nasal bridge (12 of 22) [OMIM:Narrow nasal bridge (12 of 22)]
Quality:
Cross references:
HPO:0000446 "Narrow nasal bridge" [Orphanet:8120]
Orphanet:8120 "Narrow nasal bridge" [Orphanet:8120]
OMIM: "Pinched nose" [OMIM:Pinched nose]
OMIM: "Narrow nasal bridge (12 of 22)" [OMIM:Narrow nasal bridge (12 of 22)]
Is a (Direct Parents):
HPO         Abnormality of the nasal dorsum
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 external nose(HPO:0010938)
                      Abnormality of the nasal dorsum(HPO:0011119)
                         Narrow nasal ridge(HPO:0000418)
MedDRA:
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

ALDH18A1-related De Barsy syndrome (Orphanet:35664)
Autosomal recessive cutis laxa type 2B (Orphanet:357064)
Bazex-Dupré-Christol syndrome (Orphanet:113)
CHROMOSOME 22q13 DUPLICATION SYNDROME (OMIM:615538)
De Barsy syndrome (Orphanet:2962)
Galloway-Mowat syndrome (Orphanet:2065)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
Large congenital melanocytic nevus (Orphanet:626)
Lethal restrictive dermopathy (Orphanet:1662)
Mandibuloacral dysplasia (Orphanet:2457)
Mandibuloacral dysplasia with type A lipodystrophy (Orphanet:90153)
Mandibuloacral dysplasia with type B lipodystrophy (Orphanet:90154)
Microcephalic osteodysplastic dysplasia, Saul-Wilson type (Orphanet:85172)
PYCR1-related DeBarsy syndrome (Orphanet:293633)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)