Disease Browser
|
Parent Node: Bone Diseases, Developmental (D001848) |
Parent Node: Retinitis Pigmentosa (D012174) |
..Starting node ..Skeletal Dysplasia, Rhizomelic, with Retinitis Pigmentosa (C563806)
|
Child Nodes:
|
Sister Nodes: |
..Aldred syndrome (C537046)
|
..Alstrom Syndrome (D056769)
|
..Amaurosis hypertrichosis (C536604)
|
..Bork Stender Schmidt syndrome (C536576)
|
..Chang Davidson Carlson syndrome (C538075)
|
..Chromosome Xp11.3 Deletion Syndrome (C564481)
|
..Cone Dystrophy 3 (C566579)
|
..Cone Dystrophy 4 (C567758)
|
..Cone Dystrophy, X-Linked, 1 (C564439)
|
..Cone dystrophy, x-linked, with tapetal-like sheen (C535975)
|
..Cone rod dystrophy amelogenesis imperfecta (C535976)
|
..Cone-Rod Dystrophy 1 (C563469)
|
..Cone-Rod Dystrophy 10 (C564597)
|
..Cone-Rod Dystrophy 11 (C563671)
|
..Cone-Rod Dystrophy 12 (C567206)
|
..Cone-Rod Dystrophy 13 (C567698)
|
..CONE-ROD DYSTROPHY 2 (OMIM:120970)
|
..Cone-Rod Dystrophy 3 (C565827)
|
..Cone-Rod Dystrophy 5 (C563415)
|
..Cone-Rod Dystrophy 7 (C566350)
|
..Cone-Rod Dystrophy 8 (C565322)
|
..Cone-Rod Dystrophy, X-Linked, 2 (C564717)
|
..Cone-Rod Dystrophy, X-Linked, 3 (C564507)
|
..Cone-Rod Dystrophy, X-Linked, Type 1 (C564438)
|
..Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness (C565306)
|
..Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities (C567467)
|
..Flynn Aird syndrome (C537066)
|
..Furukawa Takagi Nakao syndrome (C538193)
|
..Hardikar syndrome (C535632)
|
..Kearns-Sayre Syndrome (D007625) 1
|
..Leber Congenital Amaurosis 14 (C567636)
|
..Leber Congenital Amaurosis 3 (C565814)
|
..Light Fixation Seizure Syndrome (C566367)
|
..Mainzer-Saldino Disease (C535463)
|
..Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration (C566429)
|
..Metaphyseal Chondrodysplasia with Retinitis Pigmentosa (C565398)
|
..Microcephaly, Retinitis Pigmentosa, and Sutural Cataract (C563296)
|
..MICROPHTHALMIA, ISOLATED 5 (OMIM:611040)
|
..Microphthalmia, Posterior, With Retinitis Pigmentosa, Foveoschisis, And Optic Disc Drusen (C567024)
|
..Mirhosseini-Holmes-Walton syndrome (C538367)
|
..Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus (C562774)
|
..Neuropathy ataxia and retinis pigmentosa (C537396)
|
..Newfoundland Rod-Cone Dystrophy (C564391)
|
..Oculotrichodysplasia (C564934)
|
..Oliver-McFarlane syndrome (C536554)
|
..Pallidal Degeneration, Progressive, with Retinitis Pigmentosa (C564910)
|
..Peripheral Cone Dystrophy (C563813)
|
..Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract (C567203)
|
..Posterior column ataxia with retinitis pigmentosa (C536343)
|
..Radioulnar synostosis retinal pigment abnormalities (C536270)
|
..Retinal cone dystrophy 2 (C538363)
|
..Retinal Cone Dystrophy 3A (C566483)
|
..Retinal Cone Dystrophy 3B (C563678)
|
..Retinal Cone Dystrophy 4 (C566470)
|
..Retinitis pigmentosa 1 (C538365)
|
..Retinitis Pigmentosa 10 (C566715)
|
..Retinitis Pigmentosa 11 (C563991)
|
..Retinitis Pigmentosa 12 (C563999)
|
..Retinitis Pigmentosa 13 (C564008)
|
..Retinitis Pigmentosa 14 (C563992)
|
..Retinitis Pigmentosa 17 (C563437)
|
..Retinitis Pigmentosa 18 (C563320)
|
..Retinitis Pigmentosa 19 (C566637)
|
..Retinitis Pigmentosa 2 (C567523)
|
..Retinitis Pigmentosa 20 (C566718)
|
..Retinitis Pigmentosa 25 (C566425)
|
..Retinitis Pigmentosa 26 (C564249)
|
..Retinitis Pigmentosa 27 (C563526)
|
..Retinitis Pigmentosa 29 (C567403)
|
..Retinitis Pigmentosa 3 (C564520)
|
..Retinitis Pigmentosa 30 (C564310)
|
..Retinitis Pigmentosa 31 (C563685)
|
..Retinitis Pigmentosa 32 (C563689)
|
..Retinitis Pigmentosa 33 (C563676)
|
..Retinitis Pigmentosa 34 (C564475)
|
..Retinitis Pigmentosa 35 (C565206)
|
..Retinitis Pigmentosa 36 (C566431)
|
..Retinitis Pigmentosa 37 (C567005)
|
..Retinitis Pigmentosa 4 (C566706)
|
..Retinitis Pigmentosa 41 (C567422)
|
..Retinitis Pigmentosa 42 (C567854)
|
..Retinitis Pigmentosa 46 (C567249)
|
..RETINITIS PIGMENTOSA 50 (OMIM:613194)
|
..RETINITIS PIGMENTOSA 51 (OMIM:613464)
|
..RETINITIS PIGMENTOSA 54 (OMIM:613428)
|
..RETINITIS PIGMENTOSA 55 (OMIM:613575)
|
..RETINITIS PIGMENTOSA 56 (OMIM:613581)
|
..RETINITIS PIGMENTOSA 57 (OMIM:613582)
|
..RETINITIS PIGMENTOSA 58 (OMIM:613617)
|
..Retinitis Pigmentosa 6 (C564065)
|
..Retinitis Pigmentosa 7 (C564284)
|
..Retinitis Pigmentosa 7 With Bull'S-Eye Maculopathy (C567264)
|
..Retinitis Pigmentosa 7, Digenic (C567263)
|
..Retinitis Pigmentosa 9 (C566716)
|
..Retinitis Pigmentosa Inversa with Deafness (C564842)
|
..Retinitis Pigmentosa with Paraarteriolar Preservation Of Retinal Pigment Epithelium (C564000)
|
..Retinitis Pigmentosa, Concentric (C567712)
|
..Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism (C564841)
|
..Retinitis Pigmentosa, Late-Adult Onset (C564840)
|
..Retinitis Pigmentosa, Late-Onset Dominant (C567369)
|
..Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness (C567595)
|
..Retinitis Pigmentosa, Y-Linked (C564035)
|
..Retinopathy, Pericentral Pigmentary, Autosomal Recessive (C564838)
|
..Rhizomelic dysplasia, scoliosis, and retinitis pigmentosa (C537610)
|
..RHYNS syndrome (C537612)
|
..Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction (C564829)
|
..Senior-Loken syndrome 4 (C537581)
|
..Skeletal Dysplasia, Rhizomelic, with Retinitis Pigmentosa (C563806)
|
..Spastic Quadriplegia, Retinitis Pigmentosa, and Mental Retardation (C564808)
|
..Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy (C563825)
|
..Tapetoretinal Degeneration with Ataxia (C564788)
|
..Usher Syndromes (D052245) 19
|
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
|