Search Results

Advanced search

Link to this search: https://omia.org/results/?search_type=advanced&gb_species_id=9986&model=yes

79 phene records found

[show instead gene records]

By default, tables are sorted chronologically by Date Last Modified.

Readers can re-sort on any column by clicking on the column header. Click it again to sort in a descending order.

To create a multiple-field sort, hold down Shift while clicking on the second, third etc relevant column headers.

OMIA ID Phene Species Scientific Name Species Common Name Gene Year Key Mutation First Reported Date Last Modified
OMIA:002317-9986 Abnormal gait, retinal dysplasia, cataracts, RORB-related Oryctolagus cuniculus rabbit RORB 2021 2022-10-31
OMIA:000017-9986 Adrenal insufficiency, congenital, CYP11A1-related Oryctolagus cuniculus rabbit CYP11A1 1993 2023-09-29
OMIA:002007-9986 Agenesis, renal Oryctolagus cuniculus rabbit 2016-05-03
OMIA:001243-9986 Alkaptonuria Oryctolagus cuniculus rabbit 2018-05-31
OMIA:002600-9986 Amelogenesis imperfecta, FAM83H-related Oryctolagus cuniculus rabbit FAM83H 2022 2023-12-18
OMIA:001551-9986 Brachycephaly Oryctolagus cuniculus rabbit 2024-03-06
OMIA:000155-9986 C3 deficiency Oryctolagus cuniculus rabbit 2005-07-16
OMIA:001624-9986 C6 deficiency Oryctolagus cuniculus rabbit 2011-10-11
OMIA:000156-9986 C8 deficiency Oryctolagus cuniculus rabbit 2013-06-17
OMIA:000162-9986 Cardiomyopathy, dilated Oryctolagus cuniculus rabbit 2009-10-27
OMIA:002212-9986 Cardiomyopathy, hypertrophic, MYH7-related Oryctolagus cuniculus rabbit 2021-04-21
OMIA:002331-9986 Cardiomyopathy, TNNI3-related Oryctolagus cuniculus rabbit 2021-04-21
OMIA:002308-9986 Cardiomyopathy, X-linked dilated Oryctolagus cuniculus rabbit 2021-01-28
OMIA:002735-9986 Cataract, GJA8-related Oryctolagus cuniculus rabbit GJA8 2016 2023-12-18
OMIA:002394-9986 Cleft lip, GADD45G-related Oryctolagus cuniculus rabbit 2023-12-18
OMIA:000197-9986 Cleft palate Oryctolagus cuniculus rabbit 2005-09-06
OMIA:000201-9986 Coat colour, agouti Oryctolagus cuniculus rabbit ASIP 2010 2023-03-06
OMIA:001249-9986 Coat colour, brown, TYRP1-related Oryctolagus cuniculus rabbit TYRP1 2014 2023-03-06
OMIA:000031-9986 Coat colour, dilution, MLPH-related Oryctolagus cuniculus rabbit MLPH 2013 2023-03-06
OMIA:000209-9986 Coat colour, dominant white Oryctolagus cuniculus rabbit 2022-10-28
OMIA:001199-9986 Coat colour, extension Oryctolagus cuniculus rabbit MC1R 2006 2023-03-06
OMIA:000202-9986 Coat colour, oculocutaneous albinism type I (OCA1), TYR-related Oryctolagus cuniculus rabbit TYR 2000 2023-03-06
OMIA:001168-9986 Coronal suture synostosis Oryctolagus cuniculus rabbit 2005-09-06
OMIA:001224-9986 Craniosynostosis Oryctolagus cuniculus rabbit 2021-08-22
OMIA:001794-9986 Cystic fibrosis Oryctolagus cuniculus rabbit CFTR 2020 2024-02-21
OMIA:000279-9986 Diabetes mellitus Oryctolagus cuniculus rabbit 2023-12-10
OMIA:001709-9986 Difference of sexual development, DMRT1-related Oryctolagus cuniculus rabbit DMRT1 2023 2023-12-18
OMIA:000312-9986 Dysautonomia Oryctolagus cuniculus rabbit 2005-09-06
OMIA:002157-9986 Ectodermal dysplasia-9 Oryctolagus cuniculus rabbit HOXC13 2019 2023-12-10
OMIA:000327-9986 Ehlers-Danlos syndrome, generic Oryctolagus cuniculus rabbit 2005-07-16
OMIA:000344-9986 Epilepsy Oryctolagus cuniculus rabbit 2016-04-29
OMIA:001528-9986 Fleece variation (woolly vs hairy) Oryctolagus cuniculus rabbit 2023-10-16
OMIA:001461-9986 Gangliosidosis, GM2, type I (B variant) Oryctolagus cuniculus rabbit 2013-05-03
OMIA:000411-9986 Glaucoma, generic Oryctolagus cuniculus rabbit 2022-09-17
OMIA:000439-9986 Hair, long Oryctolagus cuniculus rabbit FGF5 2023 2023-11-15
OMIA:000459-9986 Hernia, diaphragmatic Oryctolagus cuniculus rabbit 2011-10-18
OMIA:000473-9986 Hip dysplasia Oryctolagus cuniculus rabbit 2016-04-29
OMIA:000487-9986 Hydrocephalus Oryctolagus cuniculus rabbit 2016-04-29
OMIA:000493-9986 Hydrops foetalis Oryctolagus cuniculus rabbit 2016-04-29
OMIA:000499-9986 Hypercholesterolaemia Oryctolagus cuniculus rabbit 2023-12-10
OMIA:002329-9986 Hypercholesterolaemia, PCSK9-related Oryctolagus cuniculus rabbit 2023-12-18
OMIA:001160-9986 Hyperlipidaemia Oryctolagus cuniculus rabbit LDLR 1986 2013-05-17
OMIA:002490-9986 Hyperlipidaemia/atherosclerosis, APOC3-related Oryctolagus cuniculus rabbit 2023-12-18
OMIA:002063-9986 Hyperlipidaemia/atherosclerosis, APOE-related Oryctolagus cuniculus rabbit APOE 2016 2023-12-18
OMIA:000511-9986 Hyperthyroidism Oryctolagus cuniculus rabbit 2022-09-17
OMIA:001542-9986 Hypophosphatemic rickets, autosomal recessive, 1 Oryctolagus cuniculus rabbit 2023-12-18
OMIA:000540-9986 Hypotrichosis, generic Oryctolagus cuniculus rabbit 2005-09-06
OMIA:002334-9986 Long QT syndrome, KCNE1-related Oryctolagus cuniculus rabbit 2021-04-21
OMIA:002333-9986 Long QT syndrome, KCNH2-related Oryctolagus cuniculus rabbit 2021-04-21
OMIA:002332-9986 Long QT syndrome, KCNQ1-related Oryctolagus cuniculus rabbit 2021-04-21
OMIA:000618-9986 Macrostomus Oryctolagus cuniculus rabbit 2005-09-06
OMIA:000621-9986 Malignant hyperthermia Oryctolagus cuniculus rabbit 2023-01-13
OMIA:000628-9986 Marfan syndrome Oryctolagus cuniculus rabbit FBN1 2018 2023-12-10
OMIA:000629-9986 Megacolon Oryctolagus cuniculus rabbit 2015-12-31
OMIA:002688-9986 Microcephaly, YIPF5-related Oryctolagus cuniculus rabbit YIPF5 2023 2023-12-18
OMIA:002242-9986 Muscular dystrophy, ANO5-related Oryctolagus cuniculus rabbit 2023-12-18
OMIA:000683-9986 Muscular hypertrophy (double muscling) Oryctolagus cuniculus rabbit 2023-12-12
OMIA:000715-9986 Neuroaxonal dystrophy, generic Oryctolagus cuniculus rabbit 2011-05-27
OMIA:001258-9986 Obesity Oryctolagus cuniculus rabbit 2005-09-06
OMIA:000753-9986 Osteodystrophy Oryctolagus cuniculus rabbit 2005-09-06
OMIA:000755-9986 Osteopetrosis Oryctolagus cuniculus rabbit 2016-04-29
OMIA:000783-9986 Pelger-Huet anomaly Oryctolagus cuniculus rabbit 2022-11-23
OMIA:000807-9986 Polycystic kidney disease Oryctolagus cuniculus rabbit 2011-05-27
OMIA:001213-9986 Premature senesence Oryctolagus cuniculus rabbit LMNA 2019 2024-01-18
OMIA:001566-9986 Rex coat Oryctolagus cuniculus rabbit LIPH 2011 2016-05-03
OMIA:002441-9986 Short QT syndrome, KCNH2-related Oryctolagus cuniculus rabbit 2023-12-18
OMIA:000933-9986 Spina bifida Oryctolagus cuniculus rabbit 2005-09-06
OMIA:000944-9986 Spongiform encephalopathy, susceptibility/resistance to Oryctolagus cuniculus rabbit 2020-05-15
OMIA:002067-9986 Syndactyly, type Ia Oryctolagus cuniculus rabbit 2016-10-30
OMIA:000965-9986 Syringomyelia Oryctolagus cuniculus rabbit 2016-05-03
OMIA:000985-9986 Teat / nipple, number Oryctolagus cuniculus rabbit 2021-01-13
OMIA:001013-9986 Torticollis Oryctolagus cuniculus rabbit 2022-10-29
OMIA:000770-9986 Tremor, X-linked Oryctolagus cuniculus rabbit PLP1 1994 2023-03-06
OMIA:002078-9986 Tyrosinaemia, type I Oryctolagus cuniculus rabbit 2023-12-18
OMIA:002624-9986 Usher syndrome, USH2A-related Oryctolagus cuniculus rabbit 2023-12-18
OMIA:001041-9986 Ventricular septal defect Oryctolagus cuniculus rabbit 2016-04-28
OMIA:001056-9986 Von Willebrand disease, generic Oryctolagus cuniculus rabbit 2005-09-06
OMIA:001230-9986 XY sex reversal, SRY-related Oryctolagus cuniculus rabbit SRY 2017 2023-12-18
OMIA:001079-9986 Yellow fat Oryctolagus cuniculus rabbit BCO2 2015 2023-03-06