ODCs

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5 OMIM references -
7 associated genes
9 signs/symptoms

COMMON GENES: 1

1 associated gene
No signs/symptoms info

46,XY partial gonadal dysgenesis

Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis

Citations in the biomedical literature:

46,XY partial gonadal dysgenesis		Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
	Synonym(s): - 46,XY PGD - 46,XY partial testicular dysgenesis		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare genetic disease - Rare gynecologic or obstetric disease - Rare infertility - Rare urogenital disease		Classification (Orphanet): - Rare genetic disease - Rare renal disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the genitourinary system -

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: sporadic		Epidemiological data: (no data available)

	External references: 5 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

46,XY partial gonadal dysgenesis
	Very frequent - Ambiguous genitalia - Female pseudohermaphrodism / virilisation / clitoridomegaly - Hypospadias / epispadias / bent penis - Micropenis / small penis / agenesis - Mixed gonadal dysgenesis - Testis anomalies Occasional - Cortico-adrenal hypoplasia / insufficiency - Ovary / Fallopian tube neoplasm / tumor / carcinoma / cancer (excl. teratoma / germinoma) - Testicular / seminal neoplasm / tumor / carcinoma / cancer (excl. teratoma / germinoma)
Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
(no data available)