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(HPO:0000951) | Abnormality of the skin | 147 / 7739 | ||||
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(HPO:0001939) | Abnormality of metabolism/homeostasis | 328 / 7739 | ||||
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(OMIM) | Carboxypeptidase N deficiency | 1 / 7739 | ||||
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(OMIM) | Angioedema, face, tongue, limbs | 1 / 7739 | ||||
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(HPO:0000007) | Autosomal recessive inheritance | 2538 / 7739 |