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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: Infertility, Male (D007248)
..Starting node ..SPERMATOGENIC FAILURE 2 (OMIM:108420)
Child Nodes:
Sister Nodes:
..Aromatase deficiency (C537436)
..Aspermia (D053714)
..Asthenozoospermia (D053627) 1
..Azoospermia (D053713) 4
..Catsper1-Related Nonsyndromic Male Infertility (C579978)
..Deafness, Sensorineural, And Male Infertility (C567010)
..Familial gynecomastia, due to increased aromatase activity (C000591739)
..Male Infertility with Large-Headed, Multiflagellar, Polyploid Spermatozoa (C562903)
..Oligospermia (D009845) 3
..Oligosynaptic Infertility (C562902)
..Sertoli Cell-Only Syndrome (D054331) 2
..SPERMATOGENIC FAILURE 2 (OMIM:108420)
..SPERMATOGENIC FAILURE 6 (OMIM:102530)
..Spermatogenic Failure, Nonobstructive, Y-Linked (C564030)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:

10438

Name:

SPERMATOGENIC FAILURE 2

Definition:

Alternative IDs:

ParentIDs:

MESH:D007248

TreeNumbers:

C12.294.365.700/108420

Synonyms:

ASG |ASPERMIOGENESIS FACTOR |SPGF2

Slim Mappings:

Urogenital disease (male)

Reference:

MedGen: 108420
MeSH: 108420
OMIM: 108420;

Genes:

Phenotypes

1	HP:0000006	Autosomal dominant inheritance
2	HP:0000027	Azoospermia
3	HP:0000798	Oligospermia

Disease Causing ClinVar Variants