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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: Hypogonadism (D007006)
Parent Node: Mobius Syndrome (D020331)
..Starting node ..Moebius axonal neuropathy hypogonadism (C535806)
Child Nodes:
Sister Nodes:
..Congenital facial diplegia (C531747)
..Moebius axonal neuropathy hypogonadism (C535806)
..Moebius syndrome 1 (C535807)
..Myopathy, congenital nonprogressive with Moebius and Robin sequences (C536102)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	7354
Name:	Moebius axonal neuropathy hypogonadism
Definition:
Alternative IDs:
ParentIDs:	MESH:D007006\|MESH:D020331
TreeNumbers:	C10.292.300.825/C535806 \|C16.131.077.578/C535806 \|C16.614.595/C535806 \|C19.391.482/C535806
Synonyms:
Slim Mappings:	Congenital abnormality\|Endocrine system disease\|Infant-newborn disease\|Nervous system disease
Reference:	MedGen: C535806 MeSH: C535806 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants