Prader-Willi-like syndrome
MONDO:0018354Mondo
Findings
No curated finding names Prader-Willi-like syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Prader-Willi-like syndrome is a rare, genetic, endocrine disease characterized by manifestations of a Prader-Willi syndrome phenotype (including obesity, hyperphagia, hypotonia, psychomotor delay, intellectual disability, small hands/feet, hypogonadism, growth hormone deficiency and characteristic facial features) occurring in the absence of 15q11-q13 genomic abnormalities.
Definition from the Mondo Disease Ontology (MONDO:0018354), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
1 name
Resolves to: Prader-Willi-like syndrome
- Also called
- PWS-like