Rare – Page 287 – CheckOrphan

Brachymesomelia renal syndrome

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Brachymesophalangy 2 and 5

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Brachyolmia- recessive Hobaek type

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Brachyphalangy- polydactyly- and tibial aplasia/hypoplasia

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Brachymorphism onychodysplasia dysphalangism syndrome

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Brachyolmia

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Aganglionosis- total intestinal

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Aggressive Fibromatosis

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L-arginine:glycine amidinotransferase (AGAT) deficiency

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Agammaglobulinemia- microcephaly- and severe dermatitis

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