Laryngomalacia

Symptom Information:

Symptom ID: HPO:0001601
Synonyms:
Laryngomalacia (disorder) [Orphanet:32040]
Laryngomalacia [Orphanet:32040]
Laryngomalacia [OMIM:Laryngomalacia]
Laryngomalacia [MedDRA:10060786]
Laryngomalacia (reported in 1 patient) [OMIM:Laryngomalacia (reported in 1 patient)]
Quality:
Cross references:
Orphanet:32040 "Laryngomalacia" [Orphanet:32040]
OMIM: "Laryngomalacia" [OMIM:Laryngomalacia]
OMIM: "Laryngomalacia (reported in 1 patient)" [OMIM:Laryngomalacia (reported in 1 patient)]
UMLS:C0264303 "Laryngomalacia" [HPO:0001601]
UMLS:C0264303 "Laryngomalacia" [Orphanet:32040]
Is a (Direct Parents):
HPO         Abnormality of the larynx
MedDRA Laryngeal spasm, oedema and obstruction
Orphanet Abnormality of the diaphragm
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)
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)