Phenotypes for disease #01691 (CPN1D (carboxypeptidase N deficiency (CPN1D)), OMIM:212070)

8 entries on 1 page. Showing entries 1 - 8.
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Phenotype details     

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Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

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Individual ID     
0000207398 see paper; ..., angioedema occurring once weekly, attacks lasted 24h and most often involved face and tongue, but sometimes large regions of pruritic red swellings on trunk or limbs carboxypeptidase N deficiency - Familial, autosomal recessive 65y - 54y - - Johan den Dunnen 00269572
0000257333 no information on the proband clinical phenotype - - Unknown - - - - - Christian Drouet 00361942
0000257335 no record of a clinical phenotype for the c.1150_1154dup variant - - Unknown - - - - - Christian Drouet 00361943
0000257377 Proband presenting with a clinical phenotype of CPN deficiency, i.e. association of angioedema and chronic urticaria - - Familial - - - - - Christian Drouet 00361986
0000257385 Proband presenting with a CPN deficiency clinical phenotype, i.e. association of chronic urticaria and angioedema - - Familial - - - - - Christian Drouet 00361992
0000257680 Proband presenting with chronic spontaneous urticaria and angioedema - - Familial - - - - - Christian Drouet 00362269
0000301665 best corrected visual acuity: 0.8; electroretinogram , rod: severely reduced, cone: severely reduced - dystrophy, corneoretinal, crystalline, Bietti (BCD) Familial, autosomal recessive 45y - 40y - - LOVD 00409548
0000350632 Female proband presenting with a HAE-CPN phenotype - - Familial - 36y - - - Christian Drouet 00464644
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