Woodhouse–Sakati syndrome
Woodhouse-Sakati syndrome is a multisystemic disorder characterized by hypogonadism, alopecia, diabetes mellitus, intellectual deficit and extrapyramidal signs with choreoathetoid movements and dystonia
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Woodhouse–Sakati syndrome
Summary
Woodhouse–Sakati syndrome is a rare disease[1]. It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Woodhouse–Sakati syndrome's instance of is recorded as rare disease[3].
- Woodhouse–Sakati syndrome's instance of is recorded as class of disease[4].
- Woodhouse–Sakati syndrome is a type of neurodegeneration with brain iron accumulation[5].
- Woodhouse–Sakati syndrome is a type of nervous system heredodegenerative disease[6].
- Woodhouse–Sakati syndrome is a type of autosomal recessive disease[7].
- Woodhouse–Sakati syndrome is a type of syndrome[8].
- Woodhouse–Sakati syndrome's ICD-9-CM is recorded as 759.89[9].
- Woodhouse–Sakati syndrome's health specialty is recorded as genetics[10].
- Woodhouse–Sakati syndrome's genetic association is recorded as DCAF17[11].
- Woodhouse–Sakati syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3464[12].
- Woodhouse–Sakati syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0112264[13].
- Woodhouse–Sakati syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0112264[14].
Why It Matters
Woodhouse–Sakati syndrome has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2] It is known by 8 alternative names across languages and contexts.[15]