Laryngomalacia
Symptom Information:
Symptom ID: | HPO:0001601 | ||||||
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 the respiratory system(HPO:0002086) Abnormal respiratory system morphology(HPO:0012252) Abnormality of the upper respiratory tract(HPO:0002087) Abnormality of the larynx(HPO:0001600) Laryngomalacia(HPO:0001601) MedDRA: Respiratory, thoracic and mediastinal disorders(MedDRA:10038738) Upper respiratory tract disorders (excl infections)(MedDRA:10046304) Laryngeal spasm, oedema and obstruction(MedDRA:10023855) Laryngomalacia(HPO:0001601) |
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Database Frequency: | 61 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
15q14 microdeletion syndrome | (Orphanet:261190) |
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
2q37 microdeletion syndrome | (Orphanet:1001) |
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS | (OMIM:201750) |
Adducted thumbs - arthrogryposis, Christian type | (Orphanet:2952) |
Arachnodactyly - abnormal ossification - intellectual deficit | (Orphanet:1129) |
Autosomal dominant Larsen syndrome | (Orphanet:503) |
Beta-mannosidosis | (Orphanet:118) |
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency | (Orphanet:329255) |
Blepharophimosis-intellectual deficit syndrome, Verloes type | (Orphanet:293725) |
CEREBELLOFACIODENTAL SYNDROME | (OMIM:616202) |
CHARGE syndrome | (Orphanet:138) |
Campomelic dysplasia | (Orphanet:140) |
Cardiocranial syndrome, Pfeiffer type | (Orphanet:2872) |
Cenani-Lenz syndrome | (Orphanet:3258) |
Charcot-Marie-Tooth disease | (Orphanet:166) |
Cleft palate - short stature - vertebral anomalies | (Orphanet:2015) |
Cohen syndrome | (Orphanet:193) |
Congenital laryngeal web | (Orphanet:2374) |
Congenital laryngomalacia | (Orphanet:2373) |
Costello syndrome | (Orphanet:3071) |
Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis | (Orphanet:171839) |
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies | (Orphanet:221145) |
Farber lipogranulomatosis | (Orphanet:333) |
Genitopatellar syndrome | (Orphanet:85201) |
Goldenhar syndrome | (Orphanet:374) |
Hydrolethalus | (Orphanet:2189) |
KAGAMI-OGATA SYNDROME | (OMIM:608149) |
Laryngeal abductor paralysis | (Orphanet:2808) |
Laryngeal abductor paralysis - intellectual deficit | (Orphanet:2375) |
Laryngo-tracheo-esophageal cleft | (Orphanet:2004) |
Laryngo-tracheo-esophageal cleft - pulmonary hypoplasia | (Orphanet:2005) |
Larynx atresia | (Orphanet:1202) |
Lethal Larsen-like syndrome | (Orphanet:2371) |
Marshall-Smith syndrome | (Orphanet:561) |
Maternally-inherited Leigh syndrome | (Orphanet:255210) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Non-rhizomelic chondrodysplasia punctata | (Orphanet:176) |
Orofaciodigital syndrome type 2 | (Orphanet:2751) |
Orofaciodigital syndrome type 4 | (Orphanet:2753) |
Pachyonychia congenita | (Orphanet:2309) |
Pfeiffer syndrome type 2 | (Orphanet:93259) |
Pfeiffer syndrome type 3 | (Orphanet:93260) |
Ptosis - vocal cord paralysis | (Orphanet:2997) |
Relapsing polychondritis | (Orphanet:728) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
Schinzel-Giedion syndrome | (Orphanet:798) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Short rib-polydactyly syndrome | (Orphanet:1505) |
Teebi-Shaltout syndrome | (Orphanet:3291) |
Thoracolaryngopelvic dysplasia | (Orphanet:3317) |
Toriello-Carey syndrome | (Orphanet:3338) |
Triopia | (Orphanet:3374) |
Ulnar-mammary syndrome | (Orphanet:3138) |
VACTERL/VATER association | (Orphanet:887) |
Van den Ende-Gupta syndrome | (Orphanet:2460) |
Visceral neuropathy - brain anomalies - facial dysmorphism - developmental delay | (Orphanet:73246) |
Werner syndrome | (Orphanet:902) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |
XIA-GIBBS SYNDROME | (OMIM:615829) |