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Syndrome

Donohue Syndrome

AMW:DIS:050311

Rare autosomal recessive syndrome of extreme insulin resistance due to mutations in the binding domain of INSULIN RECEPTOR. Clinical features include severe intrauterine and postnatal growth restriction, characteristic dysmorphic FACIES; HIRSUTISM; VIRILIZATION; multiple endocrine abnormalities, and early death.

Pathology clinical
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Graph assertions

Donohue Syndrome has parent Abnormalities, Multiple
Donohue Syndrome has parent Craniofacial Abnormalities
Donohue Syndrome has parent Diabetes Mellitus
Donohue Syndrome has parent Genetic Diseases, Inborn

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