Choanal stenosis

Symptom Information:

Symptom ID: HPO:0000452
Synonyms:
Coanal stenosis [HPO:0000452]
Choanal atresia [Orphanet:8630]
Choanal atresia (disorder) [Orphanet:8630]
Choanal Atresia [Orphanet:8630]
Choanal stenosis [OMIM:Choanal stenosis]
Choanal atresia [MedDRA:10008587]
Choanal atresia (in some patients) [OMIM:Choanal atresia (in some patients)]
Choanal atresia (male) [OMIM:Choanal atresia (male)]
Choanal stenosis [MedDRA:10074053]
Quality:
Cross references:
HPO:0004502 "Bilateral choanal atresia" [Orphanet:8630]
HPO:0000453 "Choanal atresia" [Orphanet:8630]
Orphanet:8630 "Choanal atresia" [Orphanet:8630]
OMIM: "Choanal stenosis" [OMIM:Choanal stenosis]
OMIM: "Choanal atresia (in some patients)" [OMIM:Choanal atresia (in some patients)]
OMIM: "Choanal atresia (male)" [OMIM:Choanal atresia (male)]
UMLS:C0008297 "Choanal Atresia" [Orphanet:8630]
Is a (Direct Parents):
Orphanet Abnormality of the nose
MedDRA Congenital upper respiratory tract disorders
HPO         Abnormality of the choanae
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 choanae(HPO:0000415)
                      Choanal stenosis(HPO:0000452)
MedDRA:
Respiratory, thoracic and mediastinal disorders(MedDRA:10038738)
    Congenital respiratory tract disorders(MedDRA:10010613)
       Congenital upper respiratory tract disorders(MedDRA:10046303)
          Choanal stenosis(HPO:0000452)
Database Frequency: 23 / 7739
Resource:

All diseases associated with this symptom:

ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS (OMIM:201750)
Acro-renal-ocular syndrome (Orphanet:959)
Antley-Bixler syndrome (Orphanet:83)
Apert syndrome (Orphanet:87)
Baller-Gerold syndrome (Orphanet:1225)
CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT (OMIM:122860)
Craniodiaphyseal dysplasia (Orphanet:1513)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Fraser syndrome (Orphanet:2052)
Hypomandibular faciocranial dysostosis (Orphanet:1790)
Intellectual deficit, X-linked - craniofacioskeletal syndrome (Orphanet:163979)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
Mandibulofacial dysostosis-microcephaly syndrome (Orphanet:79113)
Marshall-Smith syndrome (Orphanet:561)
Metaphyseal chondrodysplasia, Jansen type (Orphanet:33067)
Monosomy 18q (Orphanet:1600)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Okihiro syndrome (Orphanet:93293)
Pfeiffer syndrome (Orphanet:710)
Radial ray hypoplasia - choanal atresia (Orphanet:3026)
Schinzel-Giedion syndrome (Orphanet:798)
TREACHER COLLINS SYNDROME 2 (OMIM:613717)