Rare – Page 204 – CheckOrphan

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Autoimmune peripheral neuropathy

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Autoimmune lymphoproliferative syndrome

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Congenital short femur

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Congenital spherocytic anemia

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Autosomal dominant compelling helio ophthalmic outburst syndrome

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Patterson Stevenson syndrome

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Autoimmune polyglandular syndrome type 1

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Autoimmune progesterone dermatitis

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Congenital stenosis of cervical medullary canal

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Congenital thrombotic disease- due to Protein C deficiency

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