Bifid nasal tip

Symptom Information:

Symptom ID: HPO:0000456
Synonyms:
Notched nasal tip [HPO:0000456]
Bifid nasal tip (finding) [Orphanet:8210]
Bifid nasal tip [Orphanet:8210]
Bifid nasal tip [OMIM:Bifid nasal tip]
Bifid tip/cleft nose/supernumerary nose [Orphanet:8210]
Quality:
Cross references:
Orphanet:8210 "Bifid tip/cleft nose/supernumerary nose" [Orphanet:8210]
OMIM: "Bifid nasal tip" [OMIM:Bifid nasal tip]
UMLS:C0426428 "Bifid nasal tip" [Orphanet:8210]
Is a (Direct Parents):
HPO         Abnormality of the nasal tip
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 tip(HPO:0000436)
                         Bifid nasal tip(HPO:0000456)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant omodysplasia (Orphanet:93328)
Craniofrontonasal dysplasia (Orphanet:1520)
Frontonasal dysplasia (Orphanet:250)
Frontonasal dysplasia with alopecia and genital anomaly (Orphanet:228390)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
Oculofaciocardiodental syndrome (Orphanet:2712)
Omodysplasia (Orphanet:2733)
Orofaciodigital syndrome type 2 (Orphanet:2751)
Orofaciodigital syndrome type 8 (Orphanet:2755)
Orofaciodigital syndrome type 9 (Orphanet:141007)
Trigonocephaly - bifid nose - acral anomalies (Orphanet:3368)