GenTIGSA Gene Database on Rare Genetic Disorders
  Beta Version

Select a RGD Category for details 

RGDs registry under the 'Reproductive disorders'
Disorder Name (Total=3) Aliases Sub-Category Gene Indian Reports Link
3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency
Autosomal recessive
•Steroid 5-alpha-reductase 2 deficiency
•46,XY DSD due to 5-alpha-reductase 2 deficiency
• Pseudovaginal perineoscrotal hypospadias
•Familial incomplete male pseudohermaphroditism, type 2
•Male pseudohermaphroditism due to 5-alpha-reductase deficiency
Gonadal disorders SRD5A2 steroid 5 alpha-reductase 2
Reports
Updated as of Jul 20, 2024
PubMed
46,XY sex reversal 1
Autosomal dominant, Autosomal recessive, X-linked dominant, Y-linked
•Swyer syndrome
•46,XY complete gonadal dysgenesis
•Pure gonadal dysgenesis 46,XY
•46, XY CGD
•46, XY pure gonadal dysgenesis
•46,XY sex reversal
•Gonadal dysgenesis, XY female type
Sexual differenciation disorders SRY sex determining region Y
SOX9 SRY-box transcription factor 9
DHX37 DEAH-box helicase 37
Reports
Updated as of Jul 20, 2024
PubMed
Hydatidiform mole, recurrent, 1
Autosomal recessive
•Hydatidiform mole
•HYDM1
•Hydatidiform moles
•Hydatidiform mole, recurrent
•Gestational trophoblastic disease
•Complete hydatidiform mole
•Hydatidiform mole, complete
•Classical hydatidiform mole
•Complete molar pregnancy
•Hydatidiform moles
•Molar pregnancy
Placenta neoplasm NLRP7 NLR family pyrin domain containing 7
Reports
Updated as of Mar 30, 2026
PubMed