Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

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: Fibromatosis, Gingival (D005351)
..Starting node ..Fibromatosis, Gingival, 4 (C567028)
Child Nodes:
Sister Nodes:
..FIBROMATOSIS, GINGIVAL, 1 (OMIM:135300)
..Fibromatosis, Gingival, 2 (C565323)
..Fibromatosis, gingival, 3 (C537928)
..Fibromatosis, Gingival, 4 (C567028)
..Fibromatosis, Gingival, Type 1 (C562884)
..Fibromatosis, Gingival, with Distinctive Facies (C565567)
..Fibromatosis, Gingival, with Hypertrichosis and Mental Retardation (C565331)
..Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia (C565016)
..Jones syndrome (C535886)
..Ramon Syndrome (C535285)
..Zimmerman Laband syndrome (C536725)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4283
Name:	Fibromatosis, Gingival, 4
Definition:
Alternative IDs:	OMIM:611010
ParentIDs:	MESH:D005351
TreeNumbers:	C07.465.525.304/C567028 \|C07.465.714.258.428.200/C567028 \|C07.650.525.304/C567028 \|C16.131.850.525.304/C567028
Synonyms:	Fibromatosis, Gingival, Hereditary, 4 \|GGF4 \|GINGF4 \|HGF4
Slim Mappings:	Congenital abnormality\|Mouth disease
Reference:	MedGen: C567028 MeSH: C567028 OMIM: 611010; Genes: GINGF4;
Phenotypes
Disease Causing ClinVar Variants