Phenotypes for disease #01763 (ECTD10B (dysplasia, ectodermal, type 10B, hypohidrotic/hair/tooth, autosomal recessive (ECTD10B)), OMIM:224900)

7 entries on 1 page. Showing entries 1 - 7.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000044557 sparse hair (HP:0008070), reduced number of teeth (HP:0009804), hypohidrosis (HP:000966), facial dysmorphism (HP:0001999), diffuse palmoplantar hyperkeratosis (HP:0007447) - - Isolated (sporadic) 03y - - - - Johan den Dunnen 00057902
0000045121 hypohidrotic ectodermal dysplasia - - Familial, autosomal recessive - - - - - Sigrun Maier-Wohlfart 00058501
0000045122 hypohidrotic ectodermal dysplasia - - Familial, autosomal recessive - - - - - Sigrun Maier-Wohlfart 00058502
0000227116 hypohidrotic ectodermal dysplasia hypohidrotic ectodermal dysplasia ECTD10B Familial, X-linked dominant - - - - - Sigrun Maier-Wohlfart 00299798
0000227117 hypohidrotic ectodermal dysplasia hypohidrotic ectodermal dysplasia ECTD10B Familial, X-linked dominant - - - - - Sigrun Maier-Wohlfart 00299799
0000227118 hypohidrotic ectodermal dysplasia hypohidrotic ectodermal dysplasia ECTD10B Familial, X-linked dominant - - - - - Sigrun Maier-Wohlfart 00299800
0000227119 hypohidrotic ectodermal dysplasia hypohidrotic ectodermal dysplasia ECTD10B Familial, X-linked dominant - - - - - Sigrun Maier-Wohlfart 00299801
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