Partial androgen insensitivity syndrome
Also known as PAIS, Reifenstein syndrome, Reifenstein syndrome, partial, androgen insensitivity, partial+10 more
PAIS, Reifenstein syndrome, Reifenstein syndrome, partial, androgen insensitivity, partial, androgen insensitivity, partial, with or without breast cancer, androgen insensitivity, partial, with or without breast cancer, X-linked recessive, familial incomplete Male pseudohermaphroditism, type 1, pais, partial androgen resistance syndrome, pseudohermaphroditism, incomplete male, type I, androgen insensitivity syndrome, partial, androgen resistance syndrome, partial, incomplete male pseudohermaphroditism, type I familial incomplete male pseudohermaphroditism.
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An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
PAIS, Reifenstein syndrome, Reifenstein syndrome, partial, androgen insensitivity, partial, androgen insensitivity, partial, with or without breast cancer, androgen insensitivity, partial, with or without breast cancer, X-linked recessive, familial incomplete Male pseudohermaphroditism, type 1, pais, partial androgen resistance syndrome, pseudohermaphroditism, incomplete male, type I, androgen insensitivity syndrome, partial, androgen resistance syndrome, partial, incomplete male pseudohermaphroditism, type I familial incomplete male pseudohermaphroditism
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.