male pseudohermaphroditism due to deficiency of testicular 17,20-Desmolase

Preferred Label : male pseudohermaphroditism due to deficiency of testicular 17,20-Desmolase;

Origin ID

C564109;

UMLS CUI

C1839840;

Automatic exact mappings (from CISMeF team)
- 17 alpha-Hydroxyprogesterone aldolase deficiency (disorder) [SNOMED CT concept]
- 17 alpha-hydroxyprogesterone aldolase deficiency [SNOMED Notion]
- 46,XY sex reversal 8 [DO Concept]
- 46,xy sex reversal 8 [OMIM Phenotype]
MeSH term(s) associated for indexing
- gonadal dysgenesis, 46,xy [MeSH Descriptor]
- steroid hydroxylases [MeSH Descriptor]
Record concept(s)
- male pseudohermaphroditism due to deficiency of testicular 17,20-Desmolase [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 46,XY difference of sex development due to testicular 17,20-desmolase deficiency [ORDO Disease]
- 46,xy sex reversal 8 [OMIM Phenotype]