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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: Developmental Disabilities (D002658)
Parent Node: Fractures, Bone (D050723)
..Starting node ..Chitty Hall Webb syndrome (C535929)
Child Nodes:
Sister Nodes:
..Ankle Fractures (D064386)
..Chitty Hall Webb syndrome (C535929)
..Femoral Fractures (D005264) 2
..Fractures, Closed (D005596)
..Fractures, Comminuted (D018460)
..Fractures, Compression (D050815) 1
..Fractures, Malunited (D017759)
..Fractures, Open (D005597)
..Fractures, Spontaneous (D005598)
..Fractures, Stress (D015775)
..Fractures, Ununited (D005599) 4
..Hip Fractures (D006620) 1
..Humeral Fractures (D006810)
..Intra-Articular Fractures (D057072)
..Neurologic Disease, Infantile Multisystem, with Osseous Fragility (C564954)
..Osteoporotic Fractures (D058866)
..Osteosclerosis with Ichthyosis and Fractures (C563483)
..Periprosthetic Fractures (D057068)
..Radius Fractures (D011885) 1
..Rib Fractures (D012253)
..Shoulder Fractures (D012784)
..Skull Fractures (D012887) 7
..Spinal Fractures (D016103)
..Spinal Muscular Atrophy, Type I, with Congenital Bone Fractures (C564805)
..Tibial Fractures (D013978) 1
..Ulna Fractures (D014458) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	2082
Name:	Chitty Hall Webb syndrome
Definition:
Alternative IDs:
ParentIDs:	MESH:D002658\|MESH:D050723
TreeNumbers:	C26.404/C535929 \|F03.550.362/C535929
Synonyms:
Slim Mappings:	Mental disorder\|Wounds and injuries
Reference:	MedGen: C535929 MeSH: C535929 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants