Choanal atresia

Symptom Information:

Symptom ID: HPO:0000453
Synonyms:
Choanal atresia (disorder) [Orphanet:8630]
Choanal Atresia [Orphanet:8630]
Choanal atresia [OMIM:Choanal atresia]
Choanal atresia [Orphanet:8630]
Choanal atresia [MedDRA:10008587]
Choanal atresia (in some patients) [OMIM:Choanal atresia (in some patients)]
Choanal atresia (male) [OMIM:Choanal atresia (male)]
Quality:
Cross references:
HPO:0004502 "Bilateral choanal atresia" [Orphanet:8630]
HPO:0000452 "Choanal stenosis" [Orphanet:8630]
Orphanet:8630 "Choanal atresia" [Orphanet:8630]
OMIM: "Choanal atresia" [OMIM:Choanal atresia]
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 atresia(HPO:0000453)
MedDRA:
Respiratory, thoracic and mediastinal disorders(MedDRA:10038738)
    Congenital respiratory tract disorders(MedDRA:10010613)
       Congenital upper respiratory tract disorders(MedDRA:10046303)
          Choanal atresia(HPO:0000453)
Database Frequency: 76 / 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)
Acrocraniofacial dysostosis (Orphanet:949)
Agenesis of the corpus callosum - intellectual deficit - coloboma - micrognathia (Orphanet:52055)
Anophthalmia plus syndrome (Orphanet:1104)
Antley-Bixler syndrome (Orphanet:83)
Apert syndrome (Orphanet:87)
Arrhinia - choanal atresia - microphthalmia (Orphanet:1135)
Autosomal dominant popliteal pterygium syndrome (Orphanet:1300)
Bamforth syndrome (Orphanet:1226)
CHARGE syndrome (Orphanet:138)
CHOANAL ATRESIA AND LYMPHEDEMA (OMIM:613611)
COFFIN-SIRIS SYNDROME (OMIM:135900)
Choanal atresia - deafness - cardiac defects - dysmorphism (Orphanet:1200)
Coffin-Siris syndrome (Orphanet:1465)
Congenital sodium diarrhea (Orphanet:103908)
Cornelia de Lange syndrome (Orphanet:199)
Crouzon disease (Orphanet:207)
Crouzon syndrome - acanthosis nigricans (Orphanet:93262)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
DIAMOND-BLACKFAN ANEMIA 10 (OMIM:613309)
Diabetic embryopathy (Orphanet:1926)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Distal trisomy 18q (Orphanet:1716)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 (OMIM:129900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
Edinburgh malformation syndrome (Orphanet:1895)
Embryofetopathy due to oral anticoagulant therapy (Orphanet:1914)
Fanconi anemia (Orphanet:84)
Fronto-facio-nasal dysostosis (Orphanet:1791)
Frontonasal dysplasia (Orphanet:250)
GAPO syndrome (Orphanet:2067)
HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA (OMIM:147950)
Hallermann-Streiff syndrome (Orphanet:2108)
Holoprosencephaly (Orphanet:2162)
Hypomandibular faciocranial dysostosis (Orphanet:1790)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Imperforate oropharynx - costo vetebral anomalies (Orphanet:2759)
Intellectual deficit, X-linked - craniofacioskeletal syndrome (Orphanet:163979)
Isolated breast aplasia (Orphanet:180188)
Kallmann syndrome (Orphanet:478)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
Lethal restrictive dermopathy (Orphanet:1662)
Lowry-MacLean syndrome (Orphanet:2409)
MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES (OMIM:607597)
Mandibulofacial dysostosis-microcephaly syndrome (Orphanet:79113)
Marshall-Smith syndrome (Orphanet:561)
Metaphyseal chondrodysplasia, Jansen type (Orphanet:33067)
Methimazole embryofetopathy (Orphanet:1923)
Microcephalic primordial dwarfism due to ZNF335 deficiency (Orphanet:329228)
Microform holoprosencephaly (Orphanet:280200)
Monosomy 9p (Orphanet:261112)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Nijmegen breakage syndrome (Orphanet:647)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
Okihiro syndrome (Orphanet:93293)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Osteoglophonic dwarfism (Orphanet:2645)
Pfeiffer syndrome (Orphanet:710)
Pfeiffer syndrome type 2 (Orphanet:93259)
Pfeiffer syndrome type 3 (Orphanet:93260)
Postaxial acrofacial dysostosis (Orphanet:246)
Radial ray hypoplasia - choanal atresia (Orphanet:3026)
Schinzel-Giedion syndrome (Orphanet:798)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Solitary median maxillary central incisor syndrome (Orphanet:2286)
Syngnathia multiple anomalies (Orphanet:3262)
TREACHER COLLINS SYNDROME 2 (OMIM:613717)
Tetraamelia - multiple malformations (Orphanet:3301)
Treacher-Collins syndrome (Orphanet:861)
Trisomy 18 (Orphanet:3380)
VACTERL/VATER association (Orphanet:887)