Woodhouse-Sakati syndrome is a multisystemic disorder characterized by hypogonadism, alopecia, diabetes mellitus, intellectual deficit and extrapyramidal signs with choreoathetoid movements and dystonia.
Synonyms: Diabetes-hypogonadism-deafness-intellectual disability syndrome Diabetes-hypogonadism-hearing loss-intellectual disability syndrome
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Term information
database cross reference
- ICD-10:Q87.5 (Attributed (The ICD10 code is attributed by Orphanet))
- ICD-10:Q87.5 (NTBT (ORPHA code's Narrower Term maps to a Broader Term))
- OMIM:241080 (E (Exact mapping: the two concepts are equivalent))
- MeSH:C536742 (E (Exact mapping: the two concepts are equivalent))
- UMLS:C0342286 (E (Exact mapping: the two concepts are equivalent))
Term relations
Subclass of:
- disease
- present_in some Worldwide and has_point_prevalence_range some <1 / 1 000 000
- part_of some Rare disorder with multisystemic involvement and congenital hypogonadotropic hypogonadism
- part_of some Rare genetic syndromic intellectual disability
- has_age_of_onset some adolescent
- has_inheritance some autosomal recessive
- part_of some Rare syndromic intellectual disability
- part_of some Rare genetic diabetes mellitus
- part_of some Other rare diabetes mellitus
- present_in some Worldwide and has_cases/families_value value 25.0
- part_of some Rare disorder with hypergonadotropic hypogonadism
- part_of some Neurodegeneration with brain iron accumulation
- part_of some Rare disorder with dystonia and other neurologic or systemic manifestation
- has_age_of_onset some childhood