MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
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Parent Node:
expandotorhinolaryngologic disease (MONDO:0024623)
..Starting node
..expandgenetic otorhinolaryngologic disease ()

       Child Nodes:
........expandAase-Smith syndrome ()
........expandablepharon macrostomia syndrome ()
........expandAbruzzo-Erickson syndrome ()
........expandankyloblepharon-ectodermal defects-cleft lip/palate syndrome ()
........expandapert syndrome ()
........expandauriculocondylar syndrome ()
........expandautosomal dominant popliteal pterygium syndrome ()
........expandBartsocas-Papas syndrome ()
........expandBeckwith-Wiedemann syndrome ()
........expandBencze syndrome ()
........expandbenign paroxysmal positional nystagmus ()
........expandbinder syndrome ()
........expandblepharo-cheilo-odontic syndrome ()
........expandbranchio-oto-renal syndrome ()
........expandbranchiooculofacial syndrome ()
........expandCarey-Fineman-Ziter syndrome ()
........expandCHARGE syndrome ()
........expandcleft lip/palate-intestinal malrotation-cardiopathy syndrome ()
........expandcleft palate-lateral synechia syndrome ()
........expandcontractures-ectodermal dysplasia-cleft lip/palate syndrome ()
........expandcraniorhiny ()
........expandEEC syndrome ()
........expandfamilial thyroglossal duct cyst ()
........expandfemoral-facial syndrome ()
........expandFuhrmann syndrome ()
........expandgenito-palato-cardiac syndrome ()
........expandGoldenhar syndrome ()
........expandGordon syndrome ()
........expandHolzgreve-Wagner-Rehder syndrome ()
........expandhydrolethalus syndrome ()
........expandhypertelorism, microtia, facial clefting syndrome ()
........expandisolated congenital anosmia ()
........expandJuberg-Hayward syndrome ()
........expandLarsen syndrome ()
........expandmacrosomia-microphthalmia-cleft palate syndrome ()
........expandmacular coloboma-cleft palate-hallux valgus syndrome ()
........expandMarden-Walker syndrome ()
........expandMeniere disease ()
........expandmesomelic dwarfism-cleft palate-camptodactyly syndrome ()
........expandmotion sickness ()
........expandNager acrofacial dysostosis ()
........expandnasal dermoid cyst ()
........expandodontotrichomelic syndrome ()
........expandOTSC1 ()
........expandPai syndrome ()
........expandPallister-W syndrome ()
........expandPARC syndrome ()
........expandpostaxial acrofacial dysostosis ()
........expandProteus syndrome ()
........expandrapadilino syndrome ()
........expandretinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations ()
........expandRichieri Costa-Pereira syndrome ()
........expandRoberts syndrome ()
........expandsecond branchial cleft anomaly ()
........expandSimpson-Golabi-Behmel syndrome ()
........expandToriello-Carey syndrome ()
........expandTownes-Brocks syndrome ()
........expandTreacher-Collins syndrome ()
........expandvan den Ende-Gupta syndrome ()
........expandvelo-facial-skeletal syndrome ()
........expandventricular extrasystoles with syncopal episodes-perodactyly-robin sequence syndrome ()
........expandVerloove Vanhorick-Brubakk syndrome ()
........expandWeissenbacher-Zweymuller syndrome ()
........expandX-linked mandibulofacial dysostosis ()
........expandX-linked mixed deafness with perilymphatic gusher ()
........expandZlotogora-Ogur syndrome ()



 Sister Nodes: 
..expandautoimmune disease of ear, nose and throat ()
..expandCogan syndrome ()
..expanddisease of ear ()
..expanddisease of pharynx ()
..expandgenetic otorhinolaryngologic disease ()
..expandidiopathic bilateral vestibulopathy ()
..expandmal de Debarquement ()
..expandrare otorhinolaryngologic tumor ()
..expandrare otorhinolaryngological malformation ()
..expandrecurrent respiratory papillomatosis ()
..expandsemicircular canal dehiscence syndrome ()
..expandsilent sinus syndrome ()
..expandsyndrome or malformation associated with head and neck malformations ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:18751
Name:genetic otorhinolaryngologic disease
Definition:An instance of otorhinolaryngologic disease that is caused by a modification of the individual's genome.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:genetic otorhinolaryngologic disease
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
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