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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: Kallmann Syndrome (D017436)
Parent Node: Synkinesis (D046608)
..Starting node ..Kallmann Syndrome 2 with Bimanual Synkinesia (C563652)
Child Nodes:
Sister Nodes:
..Kallmann Syndrome 2 with Bimanual Synkinesia (C563652)
..Levator-Medial Rectus Synkinesis (C563625)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6011
Name:	Kallmann Syndrome 2 with Bimanual Synkinesia
Definition:
Alternative IDs:
ParentIDs:	MESH:D017436\|MESH:D046608
TreeNumbers:	C10.597.350.675/C563652 \|C12.706.316.096.750/C563652 \|C13.351.875.253.096.750/C563652 \|C16.131.939.316.096.750/C563652 \|C16.320.467/C563652 \|C19.391.119.096.750/C563652 \|C19.391.482.600/C563652 \|C23.888.592.350.675/C563652
Synonyms:
Slim Mappings:	Congenital abnormality\|Endocrine system disease\|Genetic disease (inborn)\|Nervous system disease\|Signs and symptoms\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: C563652 MeSH: C563652 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants