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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: Cleft Palate (D002972)
Parent Node: Genetic Diseases, X-Linked (D040181)
Parent Node: Tongue Diseases (D014060)
..Starting node ..Cleft Palate with Ankyloglossia (C564442)
Child Nodes:
Sister Nodes:
..Cleft Palate with Ankyloglossia (C564442)
..Glossalgia (D005926)
..Glossitis (D005928) 2
..Glossoptosis (D065710)
..Macroglossia (D008260) 1
..Tongue Neoplasms (D014062) 1
..Tongue, Fissured (D014063) 2
..Tongue, Hairy (D014064) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	2431
Name:	Cleft Palate with Ankyloglossia
Definition:
Alternative IDs:
ParentIDs:	MESH:D002972\|MESH:D014060\|MESH:D040181
TreeNumbers:	C05.500.460.185/C564442 \|C05.660.207.540.460.185/C564442 \|C07.320.440.185/C564442 \|C07.465.525.185/C564442 \|C07.465.910/C564442 \|C07.650.500.460.185/C564442 \|C07.650.525.185/C564442 \|C16.131.621.207.540.460.185/C564442 \|C16.131.850.500.460.185/C564442 \|C16.131.85
Synonyms:
Slim Mappings:	Congenital abnormality\|Genetic disease (inborn)\|Mouth disease\|Musculoskeletal disease
Reference:	MedGen: C564442 MeSH: C564442 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants