partial androgen insensitivity syndrome https://github.com/monarch-initiative/mondo/issues/4521 https://rarediseases.info.nih.gov/diseases/5692/partial-androgen-insensitivity-syndrome https://www.malacards.org/card/androgen_insensitivity_partial NORD:771 Reifenstein syndrome pais OMIM:307300 ICD10CM:E34.52 pseudohermaphroditism, incomplete male, type I partial androgen resistance syndrome androgen insensitivity, partial, with or without breast cancer, X-linked recessive GARD:0005692 GTR:AN0098650 GTR:AN0098651 GTR:AN0098649 UMLS:C0268301 type I familial incomplete male pseudohermaphroditism Partial androgen insensitivity syndrome (PAIS) is a disorder of sex development (DSD) distinct from complete AIS (CAIS) characterized by the presence of abnormal genital development in a 46,XY individual with normal testis development and partial responsiveness to age-appropriate levels of androgens. incomplete male pseudohermaphroditism Orphanet:90797 NCIT:C120192 MESH:C538435 OMIM:312100 androgen insensitivity, partial OMIM:312300 androgen insensitivity syndrome, partial androgen insensitivity, partial, with or without breast cancer androgen resistance syndrome, partial GTR:AN0098652 MONDO:0010720 SCTID:122811000119101 GTR:AN0098654 GTR:AN0098655 MEDGEN:82785 familial incomplete Male pseudohermaphroditism, type 1 Reifenstein syndrome, partial PAIS DOID:0080776 androgen insensitivity syndrome