Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
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Bone Diseases, Developmental (D001848)
Parent Node:
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Musculoskeletal Abnormalities (D009139)
..Starting node
..expand
Funnel Chest (D005660)

       Child Nodes:
........expandAtrial Septal Defect, Secundum, with Various Cardiac and Noncardiac Defects (C566351)
........expandPectus Excavatum, Macrocephaly, Short Stature, Dysplastic Nails (C563941)
........expandTibia, Bowing of, with Pseudarthrosis and Pectus Excavatum (C563787)
........expandZori Stalker Williams syndrome (C536728)



 Sister Nodes: 
..expandAbsent patella (C535568)
..expandACROPECTOROVERTEBRAL DYSPLASIA (OMIM:102510)
..expandArthrogryposis (D001176) Child55
..expandCampomelic Dysplasia (D055036) Child6
..expandCervical Rib Syndrome (D002573) Child1
..expandChondrodysplasia, Grebe type (C537915)
..expandCongenital absence of gluteal muscles (C535561)
..expandCongenital absence of the sternocleidomastoid muscle (C535977)
..expandCongenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi (C567863)
..expandCraniofacial Abnormalities (D019465) Child685
..expandFunnel Chest (D005660) Child4
..expandGastroschisis (D020139) Child1
..expandHajdu-Cheney Syndrome (D031845) Child1
..expandHip Dislocation, Congenital (D006618) Child12
..expandKlippel-Feil Syndrome (D007714) Child5
..expandLarsen syndrome, recessive type (C537874)
..expandLaryngomalacia (D055092) Child1
..expandLimb Deformities, Congenital (D017880) Child495
..expandPectus Carinatum (D066166)
..expandPseudoarthrogryposis (C566753)
..expandPterygium, Antecubital (C566738)
..expandSacrococcygeal dysgenesis association (C537225)
..expandSternal cleft (C537489)
..expandSynostosis (D013580) Child150
..expandTracheobronchomalacia (D055089) Child4
..expandVACTERL Association With Hydrocephalus (C564751)
..expandWidow's Peak Syndrome (C564040)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:4459
Name:Funnel Chest
Definition:A developmental anomaly in which the lower sternum is posteriorly dislocated and concavely deformed, resulting in a funnel-shaped thorax.
Alternative IDs:
ParentIDs:MESH:D001848|MESH:D009139
TreeNumbers:C05.116.099.386 |C05.660.386 |C16.131.621.386
Synonyms:Chest, Funnel |Chests, Funnel |Excavatum, Pectus |Funnel Chests |Pectus Excavatum
Slim Mappings:Congenital abnormality|Musculoskeletal disease
Reference: MedGen: D005660
MeSH: D005660
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants