Narrow naris

Symptom Information:

Symptom ID: HPO:0009933
Synonyms:
Naris, narrow [HPO:0009933]
Naris, slit-like [HPO:0009933]
Thin nares [HPO:0009933]
Small nostrils (finding) [Orphanet:8540]
Small nostrils [Orphanet:8540]
Thin nares [OMIM:Thin nares]
Small/triangular nares/nostrils [Orphanet:8540]
Quality:
Cross references:
Orphanet:8540 "Small/triangular nares/nostrils" [Orphanet:8540]
OMIM: "Thin nares" [OMIM:Thin nares]
UMLS:C0426436 "Small nostrils" [Orphanet:8540]
Is a (Direct Parents):
Orphanet Abnormality of the nose
HPO         Abnormality of the nares
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 nares(HPO:0005288)
                      Narrow naris(HPO:0009933)
MedDRA:
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

12q14 microdeletion syndrome (Orphanet:94063)
8q22.1 microdeletion syndrome (Orphanet:178303)
Brachytelephalangy - dysmorphism - Kallmann syndrome (Orphanet:1295)
Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis (Orphanet:171839)
Deafness with labyrinthine aplasia, microtia, and microdontia (Orphanet:90024)
Freeman-Sheldon syndrome (Orphanet:2053)
Gingival fibromatosis - facial dysmorphism (Orphanet:2025)
Hallermann-Streiff syndrome (Orphanet:2108)
Johanson-Blizzard syndrome (Orphanet:2315)
Maxillo-nasal dysplasia (Orphanet:1248)
Oculodentodigital dysplasia (Orphanet:2710)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Phocomelia - ectrodactyly - deafness - sinus arrhythmia (Orphanet:2878)
ROBERTS SYNDROME (OMIM:268300)
Roberts syndrome (Orphanet:3103)
Trichodental syndrome (Orphanet:3351)