Phenotypes for disease #01315 (epidermolysis bullosa, congenital localized absence of skin and nail deformity (EBD Bart type), OMIM:132000)

8 entries on 1 page. Showing entries 1 - 8.
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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     
0000187893 nails only - - Familial, autosomal dominant - - - - - Peter van den Akker 00248935
0000187894 nails only - - Familial, autosomal dominant - - - - - Peter van den Akker 00248936
0000187909 nails only - - Familial, autosomal dominant - - - - - Peter van den Akker 00248951
0000187910 nails only - - Familial, autosomal dominant - - - - - Peter van den Akker 00248952
0000187911 nails only - - Familial, autosomal dominant - - - - - Peter van den Akker 00248953
0000187927 nails only - - Familial, autosomal dominant - - - - - Peter van den Akker 00248969
0000232030 - - - Familial, autosomal dominant - - - - - Sha Hong 00306184
0000274633 Epidermolysis bullosa (Dermatological) - Epidermolysis bullosa, Bart type Familial - - - - - LOVD 00380780
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