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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Jaw Abnormalities (D007569)
Parent Node: Mandibular Diseases (D008336)
..Starting node ..Retrognathia (D063173)
Child Nodes:
........Kasznica Carlson Coppedge syndrome (C537011)
........PARC syndrome (C537174)
........Scaphocephaly, Maxillary Retrusion, And Mental Retardation (C566511)
Sister Nodes:
..Craniomandibular Disorders (D017271) 4
..Mandibular Neoplasms (D008339) 1
..Prognathism (D011378) 4
..Retrognathia (D063173) 3
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9796
Name:	Retrognathia
Definition:	A physical misalignment of the upper (maxilla) and lower (mandibular) jaw bones in which either or both recede relative to the frontal plane of the forehead.
Alternative IDs:
ParentIDs:	MESH:D007569\|MESH:D008336
TreeNumbers:	C05.500.460.827 \|C05.660.207.540.460.827 \|C07.320.440.827 \|C07.320.610.827 \|C07.650.500.460.827 \|C16.131.621.207.540.460.827 \|C16.131.850.500.460.827
Synonyms:	Mandibular Retroposition \|Mandibular Retropositions \|Mandibular Retrusion \|Mandibular Retrusions \|Maxillary Retroposition \|Maxillary Retropositions \|Maxillary Retrusion \|Maxillary Retrusions \|Retrognathias \|Retrognathism \|Retrognathisms \|Retroposition, Mandibular \|R
Slim Mappings:	Congenital abnormality\|Mouth disease\|Musculoskeletal disease
Reference:	MedGen: D063173 MeSH: D063173 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants