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Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.
Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"
Leydig cell hypoplasia due to partial LH resistance
46,XY DSD due to partial LH receptor inactivation · 46,XY DSD due to partial LH resistance
Leydig cell hypoplasia
46,XY DSD due to LH resistance or LHB deficiency · 46,XY DSD due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency
Leydig cell hypoplasia due to complete LH resistance
46,XY DSD due to complete LH receptor inactivation · 46,XY DSD due to complete LH resistance
Leydig cell hypoplasia due to LHB deficiency
46,XY DSD due to LHB deficiency · 46,XY DSD due to luteinizing hormone subunit beta deficiency
Partial androgen insensitivity syndrome
PAIS · Partial androgen resistance syndrome