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Term:
retinitis pigmentosa 51
(DOID:0110398)
Annotations:
Rat: (1)
Mouse: (1)
Human: (1)
Chinchilla: (1)
Bonobo: (1)
Dog: (1)
Squirrel: (1)
Pig: (1)
Naked Mole-rat: (1)
Green Monkey: (1)
Parent Terms
Term With Siblings
Child Terms
retinitis pigmentosa
+
Aldred Syndrome
Alstrom syndrome
Amaurosis Hypertrichosis
autosomal recessive pericentral pigmentary retinopathy
Bork Stender Schmidt Syndrome
Chang Davidson Carlson Syndrome
Chromosome Xp11.3 Deletion Syndrome
Concentric Annular Macular Dystrophy
Cone Dystrophy 4
Cone Rod Dystrophy Amelogenesis Imperfecta
cone-rod dystrophy 1
cone-rod dystrophy 10
cone-rod dystrophy 11
cone-rod dystrophy 13
cone-rod dystrophy 14
cone-rod dystrophy 16
cone-rod dystrophy 17
cone-rod dystrophy 19
cone-rod dystrophy 2
cone-rod dystrophy 20
cone-rod dystrophy 3
cone-rod dystrophy 5
cone-rod dystrophy 6
cone-rod dystrophy 7
cone-rod dystrophy 8
Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities
dominant pericentral pigmentary retinopathy
Flynn Aird Syndrome
Furukawa Takagi Nakao Syndrome
Hardikar Syndrome
INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA
isolated microphthalmia 5
Jalili syndrome
Kearns-Sayre syndrome
late-adult onset retinitis pigmentosa
Leber congenital amaurosis 14
Leber congenital amaurosis 3
Macular Dystrophy with Central Cone Involvement
Metaphyseal Chondrodysplasia with Retinitis Pigmentosa
Microcephaly, Retinitis Pigmentosa, and Sutural Cataract
Mirhosseini-Holmes-Walton Syndrome
multiple congenital anomalies-hypotonia-seizures syndrome 3
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus
NARP syndrome
Newfoundland cone-rod dystrophy
Oculotrichodysplasia
Oliver-McFarlane syndrome
Peripheral Cone Dystrophy
PHARC syndrome
Pigmentary Retinopathy and Sensorineural Deafness
Posterior Column Ataxia with Retinitis Pigmentosa
Progressive Pallidal Degeneration with Retinitis Pigmentosa
Radioulnar Synostosis Retinal Pigment Abnormalities
retinal cone dystrophy 3A
retinal cone dystrophy 3B
retinal cone dystrophy 4
retinitis pigmentosa 1
retinitis pigmentosa 10
retinitis pigmentosa 11
retinitis pigmentosa 12
retinitis pigmentosa 13
retinitis pigmentosa 14
retinitis pigmentosa 17
retinitis pigmentosa 18
retinitis pigmentosa 19
retinitis pigmentosa 2
retinitis pigmentosa 20
retinitis pigmentosa 22
retinitis pigmentosa 23
retinitis pigmentosa 24
retinitis pigmentosa 25
retinitis pigmentosa 26
retinitis pigmentosa 27
retinitis pigmentosa 28
retinitis pigmentosa 29
retinitis pigmentosa 3
retinitis pigmentosa 30
retinitis pigmentosa 31
retinitis pigmentosa 32
retinitis pigmentosa 33
retinitis pigmentosa 34
retinitis pigmentosa 35
retinitis pigmentosa 36
retinitis pigmentosa 37
retinitis pigmentosa 38
retinitis pigmentosa 39
retinitis pigmentosa 4
retinitis pigmentosa 40
retinitis pigmentosa 41
retinitis pigmentosa 42
retinitis pigmentosa 43
retinitis pigmentosa 44
retinitis pigmentosa 45
retinitis pigmentosa 46
retinitis pigmentosa 47
retinitis pigmentosa 48
retinitis pigmentosa 49
retinitis pigmentosa 50
retinitis pigmentosa 51
A retinitis pigmentosa that has_material_basis_in mutation in the TTC8 gene on chromosome 14q31. (DO)
retinitis pigmentosa 54
retinitis pigmentosa 55
retinitis pigmentosa 56
retinitis pigmentosa 57
retinitis pigmentosa 58
retinitis pigmentosa 59
retinitis pigmentosa 6
retinitis pigmentosa 60
retinitis pigmentosa 61
retinitis pigmentosa 62
retinitis pigmentosa 63
retinitis pigmentosa 66
retinitis pigmentosa 67
retinitis pigmentosa 68
retinitis pigmentosa 69
retinitis pigmentosa 7
retinitis pigmentosa 70
retinitis pigmentosa 71
retinitis pigmentosa 72
retinitis pigmentosa 73
retinitis pigmentosa 74
retinitis pigmentosa 75
Retinitis Pigmentosa 76
retinitis pigmentosa 77
Retinitis Pigmentosa 78
Retinitis Pigmentosa 79
Retinitis Pigmentosa 80
retinitis pigmentosa 81
retinitis pigmentosa 83
retinitis pigmentosa 84
retinitis pigmentosa 85
retinitis pigmentosa 86
retinitis pigmentosa 87
retinitis pigmentosa 88
retinitis pigmentosa 89
retinitis pigmentosa 9
retinitis pigmentosa 90
Retinitis Pigmentosa 92
Retinitis Pigmentosa 93
Retinitis Pigmentosa 95
Retinitis Pigmentosa 96
Retinitis Pigmentosa 97
Retinitis Pigmentosa 98
RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS
Retinitis Pigmentosa Inversa with Deafness
retinitis pigmentosa with or without situs inversus
Retinitis Pigmentosa with Paraarteriolar Preservation Of Retinal Pigment Epithelium
retinitis pigmentosa Y-linked
Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism
Retinitis Pigmentosa, Late-Onset Dominant
Rhizomelic Dysplasia, Scoliosis, and Retinitis Pigmentosa
Rhizomelic Skeletal Dysplasia with Retinitis Pigmentosa
RHYNS Syndrome
Senior-Loken Syndrome 4
Severe Mental Retardation, with Spasticity and Pigmentary Tapetoretinal Degeneration
short stature, hearing loss, retinitis pigmentosa, and distinctive facies
short-rib thoracic dysplasia 9 with or without polydactyly
Spastic Quadriplegia, Retinitis Pigmentosa, and Mental Retardation
spondylometaphyseal dysplasia with cone-rod dystrophy
Tapetoretinal Degeneration with Ataxia
Usher syndrome
+
X-Linked Cone Dystrophy with Tapetal-like Sheen
X-linked cone-rod dystrophy 1
X-linked cone-rod dystrophy 2
X-linked cone-rod dystrophy 3
X-linked retinitis pigmentosa and sinorespiratory infections
Synonyms
Exact Synonyms:
RP51
Broad Synonyms:
TTC8-RELATED CONDITION
Xrefs:
MIM:613464
;
MONDO:0013274
Definition Sources:
https://www.ncbi.nlm.nih.gov/pubmed/20451172
"DO" "DO"