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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: Mouth Abnormalities (D009056)
..Starting node ..Microstomia (D008865)
Child Nodes:
........Agnathia-microstomia-synotia (C538059)
........Faciocardiomelic Dysplasia, Lethal (C565578)
........Kniest-Like Dysplasia with Pursed Lips and Ectopia Lentis (C565452)
........Samson Viljoen syndrome (C537231)
Sister Nodes:
..Ankyloglossia (C562396)
..Calabro syndrome (C537960)
..Cleft Lip (D002971) 59
..Cleft Palate (D002972) 103
..Cleft Palate-Lateral Synechia Syndrome (C563047)
..Contractures, Congenital, Torticollis, and Malignant Hyperthermia (C565679)
..Fibromatosis, Gingival (D005351) 11
..Jagell Holmgren Hofer syndrome (C537364)
..Macrostomia (D008265) 3
..Microstomia (D008865) 4
..Taurodontism, microdontia, and dens invaginatus (C536947)
..Temtamy preaxial brachydactyly syndrome (C536958)
..Velopharyngeal Insufficiency (D014681)
..Verloove-Vanhorick Brubakk syndrome (C536541)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	7255
Name:	Microstomia
Definition:	A congenital defect in which the mouth is unusually small. (Dorland, 27th ed)
Alternative IDs:
ParentIDs:	MESH:D009056
TreeNumbers:	C07.465.525.520 \|C07.650.525.520 \|C16.131.850.525.520
Synonyms:	Microstomias
Slim Mappings:	Congenital abnormality\|Mouth disease
Reference:	MedGen: D008865 MeSH: D008865 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants