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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: 46, XY Disorders of Sex Development (D058490)
..Starting node ..Male pseudohermaphroditism due to defective LH molecule (C535692)
Child Nodes:
Sister Nodes:
..17-Hydroxysteroid Dehydrogenase Deficiency (C537805) 1
..46,Xy True Hermaphroditism, Sry-Related (C567575)
..Androgen-Insensitivity Syndrome (D013734) 2
..Denys-Drash Syndrome (D030321)
..Frasier Syndrome (D052159)
..Gonadal Dysgenesis, 46,XY (D006061) 18
..Kallmann Syndrome (D017436) 9
..Leydig Cell Hypoplasia (C562567)
..Lipoid congenital adrenal hyperplasia (C537027)
..Male pseudohermaphroditism due to defective LH molecule (C535692)
..Male pseudohermaphroditism/mental retardation syndrome, Verloes type (C535693)
..Nivelon Nivelon Mabille syndrome (C536123)
..Persistent Mullerian duct syndrome (C536665)
..Pseudovaginal Perineoscrotal Hypospadias (C535830)
..Urioste Martinez-Frias syndrome (C536478)
..WAGR Syndrome (D017624) 2
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6723
Name:	Male pseudohermaphroditism due to defective LH molecule
Definition:
Alternative IDs:
ParentIDs:	MESH:D058490
TreeNumbers:	C12.706.316.096/C535692 \|C13.351.875.253.096/C535692 \|C16.131.939.316.096/C535692 \|C19.391.119.096/C535692 \|F03.800.399.750/C535692
Synonyms:
Slim Mappings:	Congenital abnormality\|Endocrine system disease\|Mental disorder\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: C535692 MeSH: C535692 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants