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:
expandAnodontia (D000848)
Parent Node:
expandCleft Palate (D002972)
Parent Node:
expandFoot Deformities, Congenital (D005532)
Parent Node:
expandHearing Loss, Conductive (D006314)
..Starting node
..expandCleft Palate, Deafness, and Oligodontia (C565844)

       Child Nodes:



 Sister Nodes: 
..expandAbruzzo Erickson syndrome (C535559)
..expandCleft Palate, Deafness, and Oligodontia (C565844)
..expandDeafness conductive ptosis skeletal anomalies (C535993)
..expandDeafness, Cochlear, with Myopia and Intellectual Impairment (C565645)
..expandDeafness, Conductive Stapedial, with Ear Malformation and Facial Palsy (C565123)
..expandDeafness, Conductive, with Malformed External Ear (C565644)
..expandDeafness, Neural, with Atypical Atopic Dermatitis (C565639)
..expandDeafness, Progressive, With Stapes Fixation (C563316)
..expandEpiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness (C565046)
..expandGOMBO syndrome (C537284)
..expandMastocytosis, cutaneous, with short stature, conductive hearing loss and microtia (C536033)
..expandMengel Konigsmark syndrome (C537239)
..expandMetaphyseal Dysostosis, Mental Retardation, and Conductive Deafness (C565396)
..expandMicrotia, meatal atresia and conductive deafness (C537469)
..expandMitral Regurgitation, Conductive Deafness, and Fusion of Cervical Vertebrae and of Carpal and Tarsal Bones (C563572)
..expandProgressive hearing loss stapes fixation (C536424)
..expandRetinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism (C564841)
..expandSchweitzer Kemink Graham syndrome (C536511)
..expandSiegler Brewer Carey syndrome (C537335)
..expandStoll Levy Francfort syndrome (C537498)
..expandZunich neuroectodermal syndrome (C536729)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:2427
Name:Cleft Palate, Deafness, and Oligodontia
Definition:
Alternative IDs:
ParentIDs:MESH:D000848|MESH:D002972|MESH:D005532|MESH:D006314
TreeNumbers:C05.330.495/C565844 |C05.500.460.185/C565844 |C05.660.207.540.460.185/C565844 |C05.660.585.512.380/C565844 |C07.320.440.185/C565844 |C07.465.525.185/C565844 |C07.650.500.460.185/C565844 |C07.650.525.185/C565844 |C07.650.800.100/C565844 |C07.793.700.100/C565844 |C0
Synonyms:
Slim Mappings:Congenital abnormality|Ear-nose-throat disease|Mouth disease|Musculoskeletal disease|Nervous system disease|Signs and symptoms
Reference: MedGen: C565844
MeSH: C565844
OMIM: 216300;

Genes:
Phenotypes
1 HP:0000007Autosomal recessive inheritance
2 HP:0008513Bilateral conductive hearing impairment
3 HP:0000185Cleft soft palate
4 HP:0008498No permanent dentition
5 HP:0012225Oligodontia of primary teeth
6 HP:0001852Sandal gap
7 HP:0010109Short hallux
Disease Causing ClinVar Variants