| Disease Browser
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Parent Node:
 Cholestasis (D002779) |
Parent Node:
Cleft Palate (D002972) |
Parent Node:
Retinitis Pigmentosa (D012174) |
..Starting node
.. Hardikar syndrome (C535632)
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Child Nodes:
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Sister Nodes: |
..Aldred syndrome (C537046)
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..Alstrom Syndrome (D056769)
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..Amaurosis hypertrichosis (C536604)
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..Bork Stender Schmidt syndrome (C536576)
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..Chang Davidson Carlson syndrome (C538075)
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..Chromosome Xp11.3 Deletion Syndrome (C564481)
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..Cone Dystrophy 3 (C566579)
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..Cone Dystrophy 4 (C567758)
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..Cone Dystrophy, X-Linked, 1 (C564439)
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..Cone dystrophy, x-linked, with tapetal-like sheen (C535975)
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..Cone rod dystrophy amelogenesis imperfecta (C535976)
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..Cone-Rod Dystrophy 1 (C563469)
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..Cone-Rod Dystrophy 10 (C564597)
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..Cone-Rod Dystrophy 11 (C563671)
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..Cone-Rod Dystrophy 12 (C567206)
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..Cone-Rod Dystrophy 13 (C567698)
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..CONE-ROD DYSTROPHY 2 (OMIM:120970)
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..Cone-Rod Dystrophy 3 (C565827)
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..Cone-Rod Dystrophy 5 (C563415)
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..Cone-Rod Dystrophy 7 (C566350)
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..Cone-Rod Dystrophy 8 (C565322)
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..Cone-Rod Dystrophy, X-Linked, 2 (C564717)
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..Cone-Rod Dystrophy, X-Linked, 3 (C564507)
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..Cone-Rod Dystrophy, X-Linked, Type 1 (C564438)
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..Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness (C565306)
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..Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities (C567467)
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..Flynn Aird syndrome (C537066)
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..Furukawa Takagi Nakao syndrome (C538193)
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..Hardikar syndrome (C535632)
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..Kearns-Sayre Syndrome (D007625)  1
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..Leber Congenital Amaurosis 14 (C567636)
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..Leber Congenital Amaurosis 3 (C565814)
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..Light Fixation Seizure Syndrome (C566367)
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..Mainzer-Saldino Disease (C535463)
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..Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration (C566429)
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..Metaphyseal Chondrodysplasia with Retinitis Pigmentosa (C565398)
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..Microcephaly, Retinitis Pigmentosa, and Sutural Cataract (C563296)
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..MICROPHTHALMIA, ISOLATED 5 (OMIM:611040)
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..Microphthalmia, Posterior, With Retinitis Pigmentosa, Foveoschisis, And Optic Disc Drusen (C567024)
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..Mirhosseini-Holmes-Walton syndrome (C538367)
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..Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus (C562774)
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..Neuropathy ataxia and retinis pigmentosa (C537396)
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..Newfoundland Rod-Cone Dystrophy (C564391)
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..Oculotrichodysplasia (C564934)
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..Oliver-McFarlane syndrome (C536554)
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..Pallidal Degeneration, Progressive, with Retinitis Pigmentosa (C564910)
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..Peripheral Cone Dystrophy (C563813)
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..Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract (C567203)
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..Posterior column ataxia with retinitis pigmentosa (C536343)
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..Radioulnar synostosis retinal pigment abnormalities (C536270)
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..Retinal cone dystrophy 2 (C538363)
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..Retinal Cone Dystrophy 3A (C566483)
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..Retinal Cone Dystrophy 3B (C563678)
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..Retinal Cone Dystrophy 4 (C566470)
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..Retinitis pigmentosa 1 (C538365)
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..Retinitis Pigmentosa 10 (C566715)
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..Retinitis Pigmentosa 11 (C563991)
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..Retinitis Pigmentosa 12 (C563999)
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..Retinitis Pigmentosa 13 (C564008)
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..Retinitis Pigmentosa 14 (C563992)
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..Retinitis Pigmentosa 17 (C563437)
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..Retinitis Pigmentosa 18 (C563320)
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..Retinitis Pigmentosa 19 (C566637)
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..Retinitis Pigmentosa 2 (C567523)
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..Retinitis Pigmentosa 20 (C566718)
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..Retinitis Pigmentosa 25 (C566425)
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..Retinitis Pigmentosa 26 (C564249)
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..Retinitis Pigmentosa 27 (C563526)
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..Retinitis Pigmentosa 29 (C567403)
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..Retinitis Pigmentosa 3 (C564520)
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..Retinitis Pigmentosa 30 (C564310)
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..Retinitis Pigmentosa 31 (C563685)
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..Retinitis Pigmentosa 32 (C563689)
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..Retinitis Pigmentosa 33 (C563676)
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..Retinitis Pigmentosa 34 (C564475)
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..Retinitis Pigmentosa 35 (C565206)
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..Retinitis Pigmentosa 36 (C566431)
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..Retinitis Pigmentosa 37 (C567005)
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..Retinitis Pigmentosa 4 (C566706)
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..Retinitis Pigmentosa 41 (C567422)
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..Retinitis Pigmentosa 42 (C567854)
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..Retinitis Pigmentosa 46 (C567249)
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..RETINITIS PIGMENTOSA 50 (OMIM:613194)
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..RETINITIS PIGMENTOSA 51 (OMIM:613464)
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..RETINITIS PIGMENTOSA 54 (OMIM:613428)
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..RETINITIS PIGMENTOSA 55 (OMIM:613575)
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..RETINITIS PIGMENTOSA 56 (OMIM:613581)
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..RETINITIS PIGMENTOSA 57 (OMIM:613582)
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..RETINITIS PIGMENTOSA 58 (OMIM:613617)
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..Retinitis Pigmentosa 6 (C564065)
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..Retinitis Pigmentosa 7 (C564284)
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..Retinitis Pigmentosa 7 With Bull'S-Eye Maculopathy (C567264)
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..Retinitis Pigmentosa 7, Digenic (C567263)
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..Retinitis Pigmentosa 9 (C566716)
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..Retinitis Pigmentosa Inversa with Deafness (C564842)
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..Retinitis Pigmentosa with Paraarteriolar Preservation Of Retinal Pigment Epithelium (C564000)
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..Retinitis Pigmentosa, Concentric (C567712)
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..Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism (C564841)
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..Retinitis Pigmentosa, Late-Adult Onset (C564840)
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..Retinitis Pigmentosa, Late-Onset Dominant (C567369)
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..Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness (C567595)
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..Retinitis Pigmentosa, Y-Linked (C564035)
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..Retinopathy, Pericentral Pigmentary, Autosomal Recessive (C564838)
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..Rhizomelic dysplasia, scoliosis, and retinitis pigmentosa (C537610)
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..RHYNS syndrome (C537612)
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..Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction (C564829)
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..Senior-Loken syndrome 4 (C537581)
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..Skeletal Dysplasia, Rhizomelic, with Retinitis Pigmentosa (C563806)
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..Spastic Quadriplegia, Retinitis Pigmentosa, and Mental Retardation (C564808)
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..Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy (C563825)
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..Tapetoretinal Degeneration with Ataxia (C564788)
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..Usher Syndromes (D052245) 19
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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