Also known as: Aldrich syndrome, Imd 2, WAS, Wiskott Aldrich syndrome, Wiskott syndrome, Wiskott-Aldrich syndrome, Wiskott-Aldrich syndrome 1, Wiskott-Aldrich syndrome, X-linked recessive, eczema thrombocytopenia immunodeficiency syndrome, eczema-thrombocytopenia-immunodeficiency syndrome, immunodeficiency 2
Also known as: IDDM-MED syndrome, Iddm-Med syndrome, MED-IDDM syndrome, Med-Iddm syndrome, WRS, Wolcott Rallison syndrome, Wolcott-Rallison syndrome, early-onset diabetes mellitus with multiple epiphyseal dysplasia, epiphyseal dysplasia multiple with early-onset diabetes mellitus, epiphyseal dysplasia, multiple, with early-onset diabetes mellitus
Also known as: WFSL, Wolfram-like syndrome, Wolfram-like syndrome, autosomal dominant, hearing loss, progressive, with optic atrophy and/or impaired glucose Regulation
Also known as: Woodhouse-Sakati syndrome, diabetes-hypogonadism-deafness-intellectual disability syndrome, extrapyramidal disorder, progressive, with primary hypogonadism, intellectual disability, and alopecia, extrapyramidal disorder, progressive, with primary hypogonadism, mental retardation, and alopecia, hypogonadism, alopecia, diabetes mellitus, intellectual disability, deafness, and extrapyramidal syndrome, hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and extrapyramidal syndrome, hypogonadism, diabetes mellitus, alopecia, intellectual disability, and electrocardiographic abnormalities, hypogonadism, diabetes mellitus, alopecia, mental retardation, and electrocardiographic abnormalities, woodhouse Sakati syndrome, woodhouse-Sakati syndrome
Also known as: wooly hair nevus
Also known as: KWWH type IV, PPKWH, keratoderma with woolly hair type IV, keratoderma with wooly hair type IV, palmoplantar keratoderma and woolly hair, palmoplantar keratoderma and wooly hair, woolly hair-palmoplantar hyperkeratosis syndrome, wooly hair-palmoplantar hyperkeratosis syndrome
Also known as: ARWH3, KRT25 woolly hair (disease), KRT25 wooly hair (disease), woolly hair (disease) caused by mutation in KRT25, woolly hair, autosomal recessive 3, with hypotrichosis, woolly hair, autosomal recessive type 3, wooly hair (disease) caused by mutation in KRT25, wooly hair, autosomal recessive 3, wooly hair, autosomal recessive 3, with hypotrichosis, wooly hair, autosomal recessive type 3
Also known as: Suarez-Stickler syndrome, cortical defects wormian bones and dentinogenesis imperfecta, cortical defects, WORMIAN bones, and dentinogenesis imperfecta
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