Phenotypes for disease #04378 (BBS5 (Bardet-Biedl syndrome, type 5 (BBS-5)), OMIM:615983)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000050418 - - - Familial, autosomal recessive - 47y - - - Muhammad Ajmal 00063830
0000210915 Obesity Rod cone dystrophy Polydactyly ID Renal abnormalities Developmental delay Diabetes mellitus Dental abnormalities Behavioral problems Facial dysmorphism - BBS5 Familial, autosomal recessive 14y 14y 14y - - Evren Gümüş 00276324
0000326685 Obesity HP:0001513, Postaxial polydactyly HP:0100259, Intellectual disability HP:0001249, Hypogonadism HP:0000135, Acanthosis nigricans HP:0000956, Reduced visual acuity HP:0007663, Nyctalopia HP:0000662, Peripheral visual field loss HP:0007994, Retinitis pigmentosa HP:0000510 Retinitis pigmentosa # 615983 Familial, autosomal recessive 10y 20y 06y - - Rocio Villafuerte-de la Cruz 00436507
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