Prader-Willi-like syndrome

MONDO:0018354

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.

Also known as: PWS-like

0 clinical trials for this condition and its sub-types, 0 tagged with Prader-Willi-like syndrome itself.

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Part of

↑ Hereditary neurological disease (5772) ↑ Congenital nervous system disorder (284) ↑ Multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome (90) ↑ Congenital hypogonadotropic hypogonadism (82)

Sub-types of Prader-Willi-like syndrome

6q16 deletion syndrome 0 trials
BDV syndrome 0 trials
SIM1-related Prader-Willi-like syndrome 0 trials

Including sub-types (0) Tagged with Prader-Willi-like syndrome (0)

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