Choanal atresia
Symptom Information:
Symptom ID: | HPO:0000453 | |||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |