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

Official abbreviation BBS5
Name Bardet-Biedl syndrome, type 5 (BBS-5)
OMIM ID 615983
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene BBS5
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00063830 - - - M yes Pakistan - - - - - BBS5 - BBS5 BBS5 1 1 Muhammad Ajmal
00276324 - - - M yes Turkey - 14y - - - BBS5 Obesity Rod cone dystrophy Polydactyly ID Renal abnormalities Developmental delay Diabetes mellitus Dental abnormalities Behavioral problems Facial dysmorphism BBS5 BBS5 1 2 Evren Gümüş
00436507 2487444 Villafuerte-de la Cruz RA, et al., 2023. Submitted - F yes Mexico Hispanic - - - None BBS5 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 BBS5 BBS5 1 1 Rocio Villafuerte-de la Cruz
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