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:
expandGrowth Disorders (D006130)
Parent Node:
expandHydrocephalus (D006849)
Parent Node:
expandJoint Instability (D007593)
Parent Node:
expandKyphosis (D007738)
Parent Node:
expandScoliosis (D012600)
..Starting node
..expandDaish Hardman Lamont syndrome (C535770)

       Child Nodes:



 Sister Nodes: 
..expandAcrodysplasia scoliosis (C538180)
..expandCervical Hypertrichosis with Underlying Kyphoscoliosis (C566142)
..expandCoffin syndrome 1 (C536435)
..expandDaish Hardman Lamont syndrome (C535770)
..expandDislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, And Mental Retardation (C566408)
..expandGaze Palsy, Familial Horizontal, with Progressive Scoliosis (C564593)
..expandIida Kannari syndrome (C536284)
..expandKyphoscoliosis 1 (C565711)
..expandMacrocephaly, Alopecia, Cutis Laxa, and Scoliosis (C567770)
..expandOmphalocele exstrophy imperforate anus (C537748)
..expandParastremmatic dwarfism (C537172)
..expandPilotto syndrome (C537400)
..expandPrata Libéral Gonçalves syndrome (C538277)
..expandRhizomelic dysplasia, scoliosis, and retinitis pigmentosa (C537610)
..expandRigid spine syndrome (C535683)
..expandScoliosis, Arachnodactyly, And Blindness (C567309)
..expandSCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 1 (OMIM:181800)
..expandSCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 2 (OMIM:607354)
..expandSCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 3 (OMIM:608765)
..expandSCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 4 (OMIM:612238)
..expandSCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 5 (OMIM:612239)
..expandShprintzen omphalocele syndrome (C537329)
..expandSpondylocarpotarsal synostosis (C535780)
..expandTsukahara Syndrome (C566376)
..expandWaaler Aarskog syndrome (C536461)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:2962
Name:Daish Hardman Lamont syndrome
Definition:
Alternative IDs:
ParentIDs:MESH:D006130|MESH:D006849|MESH:D007593|MESH:D007738|MESH:D012600
TreeNumbers:C05.116.900.800.500/C535770 |C05.116.900.800.875/C535770 |C05.550.521/C535770 |C10.228.140.602/C535770 |C10.228.140.631.450/C535770 |C23.550.393/C535770
Synonyms:Hydrocephalus, tall stature, joint laxity, and kyphoscoliosis
Slim Mappings:Musculoskeletal disease|Nervous system disease|Pathology (process)
Reference: MedGen: C535770
MeSH: C535770
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants