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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Absent Patella 
acquired laryngomalacia 
acromesomelic dysplasia, Grebe type  
agnathia-otocephaly complex  
amyotrophic lateral sclerosis type 21  
Antecubital Pterygium 
arthrogryposis multiplex congenita +   
articular cartilage disease +   
Asrar Facharzt Haque Syndrome  
autosomal dominant congenital deafness with onychodystrophy  
autosomal recessive congenital ichthyosis +   
autosomal recessive cutis laxa type IC  
bladder exstrophy-epispadias-cloacal exstrophy complex +   
blepharophimosis +   
BLISTERING, ACANTHOLYTIC, OF ORAL AND LARYNGEAL MUCOSA  
campomelic dysplasia +   
cartilage cancer 
caudal regression syndrome  
Cervical Rib Syndrome +  
cleft palate-lateral synechia syndrome  
CLOVES syndrome  
Cohen-Gibson Syndrome  
Compton-North congenital myopathy  
Congenital Absence of Gluteal Muscles 
Congenital Absence of the Sternocleidomastoid Muscle 
congenital adrenal hyperplasia +   
congenital adrenal insufficiency  
congenital afibrinogenemia +   
congenital amegakaryocytic thrombocytopenia +   
congenital aphakia  
congenital bilateral absence of vas deferens +   
congenital bile acid synthesis defect +   
congenital central hypoventilation syndrome +   
congenital chylothorax  
congenital contractural arachnodactyly  
congenital diaphragmatic hernia +   
congenital diarrhea +   
congenital disorder of glycosylation +   
congenital epulis 
congenital fibrosarcoma  
congenital fibrosis of the extraocular muscles +   
Congenital Foot Deformities +   
congenital generalized lipodystrophy +   
congenital granular cell tumor 
congenital heart block +   
CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME  
congenital heart disease +   
congenital hemolytic anemia +   
congenital hereditary endothelial dystrophy of cornea  
Congenital Hip Dislocation +   
congenital hypogammaglobulinemia 
congenital hypoplastic anemia +   
congenital hypothyroidism +   
congenital hypotrichosis with juvenile macular dystrophy  
congenital intrinsic factor deficiency  
congenital lactase deficiency  
congenital leptin deficiency  
Congenital Limb Deformities +   
congenital megabladder  
congenital mesoblastic nephroma +   
congenital mirror movement disorder +   
congenital muscular dystrophy +   
congenital myasthenic syndrome +   
congenital myopathy 4A +   
congenital nervous system abnormality +   
congenital nystagmus +   
Congenital Partial Atresia of Larynx 
congenital ptosis +   
congenital stationary night blindness +   
congenital stromal corneal dystrophy  
congenital structural myopathy +   
congenital sucrase-isomaltase deficiency  
congenital syphilis +  
congenital toxoplasmosis  
Craniofacial Abnormalities +   
cryptophthalmia +   
discitis 
epidermolysis bullosa with congenital localized absence of skin and deformity of nails  
Female Pseudohermaphroditism with Skeletal Anomalies 
Fibrocartilaginous Embolism 
Funnel Chest +   
gastroschisis +   
Hajdu-Cheney syndrome  
hypospadias +   
IMAGAWA-MATSUMOTO SYNDROME  
Immunoskeletal Dysplasia with Neurodevelopmental Abnormalities  
imperforate anus +   
Intellectual Developmental Disorder with Nasal Speech, Dysmorphic Facies, and Variable Skeletal Anomalies  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND VARIABLE SKELETAL ANOMALIES  
Iridogoniodysgenesis and Skeletal Anomalies 
Junctional Epidermolysis Bullosa 2C, Laryngoonychocutaneous  
Keutel Syndrome  
Kleefstra syndrome 2  
Klippel-Feil syndrome +   
large congenital melanocytic nevus  
Laryngeal Atresia, Encephalocele, and Limb Deformities 
Laryngeal Edema 
Laryngeal Granuloma 
Laryngeal Neoplasms +   
Laryngeal Nerve Injuries +  
laryngitis +  
Laryngocele 
laryngomalacia +   
A laryngeal disease that is characterized by inward collapse of flaccid supraglottic structures during inspiration. The most common symptom is noisy breathing (stridor) that is often worse when the infant is on his/her back or crying. (DO)
Laryngopharyngeal Reflux +  
laryngostenosis 
Leber congenital amaurosis +   
lethal congenital contracture syndrome +   
lethal congenital glycogen storage disease of heart  
Meckel's diverticulum 
microcephaly, short stature, and limb abnormalities  
MLS syndrome +   
multiple congenital anomalies-hypotonia-seizures syndrome +   
myotonia congenita +   
neural tube defect +   
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, DYSMORPHIC FACIES, AND SKELETAL ANOMALIES, WITH OR WITHOUT SEIZURES  
NEURODEVELOPMENTAL DISORDER WITH NEUROMUSCULAR AND SKELETAL ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH POOR GROWTH AND SKELETAL ANOMALIES  
NEUROFACIOSKELETAL SYNDROME WITH OR WITHOUT RENAL AGENESIS  
non-congenital cyst of kidney 
nonsyndromic congenital nail disorder +   
omphalocele  
OPHTHALMOPLEGIA, EXTERNAL, WITH RIB AND VERTEBRAL ANOMALIES  
orofacial cleft +   
Osteochondritis +   
osteochondrodysplasia +   
palmoplantar keratoderma and congenital alopecia 1  
palmoplantar keratoderma and congenital alopecia 2 
Pectus Carinatum  
Poland syndrome 
polydactyly +   
primary congenital glaucoma +   
Pseudoarthrogryposis 
radioulnar synostosis +   
rapidly involuting congenital hemangioma 
Sacral Agenesis with Vertebral Anomalies  
Sacrococcygeal Dysgenesis Association 
severe congenital encephalopathy due to MECP2 mutation  
severe congenital neutropenia +   
Short Stature with Nonspecific Skeletal Abnormalities 1  
Silver-Russell syndrome +   
spondyloepiphyseal dysplasia with congenital joint dislocations  
Steel Syndrome  
Sternal Cleft 
Stolerman neurodevelopmental syndrome  
Supraglottitis +  
synostosis +   
T-cell immunodeficiency, congenital alopecia, and nail dystrophy  
Tietze's syndrome  
TORCH syndrome 
Tracheobronchomalacia +   
visceral heterotaxy +   
Vocal Cord Dysfunction +  
Vocal Cord Paralysis +   
Voice Disorders +   
Widow's Peak Syndrome 
Zika virus congenital syndrome 
ZTTK syndrome  

Synonyms
Exact Synonyms: chondromalacia of larynx ;   congenital laryngomalacia ;   laryngomalacias ;   larynx chondromalacia ;   larynx chondromalacias
Primary IDs: MESH:D055092
Alternate IDs: MIM:150280
Xrefs: GARD:6865 ;   ICD10CM:Q31.5 ;   ORDO:2373
Definition Sources: https://www.childrenshospital.org/conditions-and-treatments/conditions/l/laryngomalacia "DO" "DO", https://www.childrenshospitalvanderbilt.org/medical-conditions/laryngomalacia "DO" "DO"

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