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:
expandAbnormalities, Drug-Induced (D000014)
Parent Node:
expandAbnormalities, Multiple (D000015)
Parent Node:
expandBone Diseases (D001847)
Parent Node:
expandCleft Palate (D002972)
Parent Node:
expandHeart Defects, Congenital (D006330)
Parent Node:
expandHip Dislocation, Congenital (D006618)
Parent Node:
expandMicrognathism (D008844)
..Starting node
..expandHo Kaufman Mcalister syndrome (C538325)

       Child Nodes:



 Sister Nodes: 
..expandBaetz-Greenwalt syndrome (C537795)
..expandBird headed dwarfism Montreal type (C535448)
..expandCerebral Cavernous Malformations 2 (C566394)
..expandCerebral Cavernous Malformations 3 (C566393)
..expandCerebrocostomandibular Syndrome (C562538)
..expandClavicular Hypoplasia, Zygomatic Arch Hypoplasia, and Micrognathia (C565729)
..expandCoffin-Siris syndrome (C536436)
..expandCorpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia (C564509)
..expandCrumpled helices and small mouth (C536217)
..expandEctrodactyly of Lower Limbs, Congenital Heart Defect, and Micrognathia (C563344)
..expandGenee-Wiedemann syndrome (C537680)
..expandGenito palato cardiac syndrome (C537683)
..expandHo Kaufman Mcalister syndrome (C538325)
..expandLimb Deficiencies, Distal, with Micrognathia (C565437)
..expandMeier-Gorlin syndrome (C538012)
..expandMilner Khallouf Gibson syndrome (C537473)
..expandMultiple Epiphyseal Dysplasia with Robin Phenotype (C563291)
..expandSchweitzer Kemink Graham syndrome (C536511)
..expandTrigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet (C564759)
..expandYunis Varon syndrome (C536719)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:5236
Name:Ho Kaufman Mcalister syndrome
Definition:
Alternative IDs:
ParentIDs:MESH:D000014|MESH:D000015|MESH:D001847|MESH:D002972|MESH:D006330|MESH:D006618|MESH:D008844
TreeNumbers:C05.116/C538325 |C05.500.460.185/C538325 |C05.500.460.457/C538325 |C05.660.207.540.460.185/C538325 |C05.660.207.540.460.457/C538325 |C05.660.449/C538325 |C07.320.440.185/C538325 |C07.320.440.457/C538325 |C07.465.525.185/C538325 |C07.650.500.460.185/C538325 |C07.65
Synonyms:
Slim Mappings:Cardiovascular disease|Congenital abnormality|Mouth disease|Musculoskeletal disease
Reference: MedGen: C538325
MeSH: C538325
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants