gonadal dysgenesis, hypergonadotropic, XX type, short stature, and recurrent metabolic acidosis

Preferred Label : gonadal dysgenesis, hypergonadotropic, XX type, short stature, and recurrent metabolic acidosis;

Origin ID

C565295;

UMLS CUI

C3148970;

Automatic exact mappings (from CISMeF team)
- Ovarian dysgenesis, hypergonadotropic, with short stature and recurrent metabolic acidosis [OMIM Phenotype]
MeSH term(s) associated for indexing
- acidosis [MeSH Descriptor]
- gonadal dysgenesis, 46,xx [MeSH Descriptor]
- growth disorders [MeSH Descriptor]
- hypogonadism [MeSH Descriptor]
- ovary [MeSH Descriptor]
Record concept(s)
- gonadal dysgenesis, hypergonadotropic, XX type, short stature, and recurrent metabolic acidosis [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ovarian dysgenesis, hypergonadotropic, with short stature and recurrent metabolic acidosis [OMIM Phenotype]