| Disease Browser
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Parent Node:
 Abnormalities, Multiple (D000015) |
Parent Node:
Eye Abnormalities (D005124) |
..Starting node
.. Oculorenocerebellar syndrome (C537739)
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Child Nodes:
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Sister Nodes: |
..Ablepharon macrostomia syndrome (C535557)
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..Aniridia (D015783)  10
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..Ankyloblepharon filiforme adnatum cleft palate (C536373)
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..Anophthalmos (D000853) 8
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..Anterior segment mesenchymal dysgenesis (C537775)
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..Asymmetric Short Stature Syndrome (C566248)
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..Axenfeld-Rieger anomaly with cardiac defects and sensorineural hearing loss (C537789)
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..Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities (C566234)
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..Axenfeld-Rieger syndrome (C535679) 3
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..Blepharophimosis (D016569) 17
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..Blue diaper syndrome (C536239)
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..Brachymetapody-Anodontia-Hypotrichosis-Albinoidism (C565893)
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..Chemke Oliver Mallek syndrome (C535922)
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..Chromosome 6pter-P24 Deletion Syndrome (C567239)
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..CODAS syndrome (C536434)
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..Cole Carpenter syndrome (C535963)
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..Coloboma (D003103) 43
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..Craniosynostosis with Ocular Abnormalities and Hallucal Defects (C564263)
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..Cryptophthalmos, Unilateral or Bilateral, Isolated (C565138)
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..Dwarfism stiff joint ocular abnormalities (C535724)
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..Ectopia Lentis (D004479) 13
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..FACES syndrome (C536384)
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..Foveal Hypoplasia and Anterior Segment Dysgenesis (C563774)
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..Fraser Syndrome (D058497)
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..Fronto-facio-nasal dysplasia (C538063)
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..Frontoocular Syndrome (C565340)
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..Goniodysgenesis-Mental Retardation-Short Stature Syndrome (C564214)
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..Hay-Wells syndrome (C535847)
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..Hydrophthalmos (D006871)
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..Iridogoniodysgenesis and skeletal anomalies (C535534)
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..Iridogoniodysgenesis type1 (C535535)
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..Iridogoniodysgenesis, dominant type (C535536)
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..Jejunal Atresia with Microcephaly and Ocular Anomalies (C565460)
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..Joubert syndrome 1 (C536293)
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..Joubert syndrome 2 (C536294)
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..Joubert Syndrome 9 (C567364)
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..Kapur Toriello syndrome (C537008)
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..Kaufman oculocerebrofacial syndrome (C537013)
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..Macrophthalmia, Colobomatous, with Microcornea (C566533)
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..Maxillofacial Dysostosis (C563599)
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..Mesangial Sclerosis, Diffuse Renal, with Ocular Abnormalities (C565405)
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..Microcornea, glaucoma, and absent frontal sinuses (C537552)
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..Microphthalmos (D008850) 57
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..MOMES Syndrome (C564660)
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..Nephrotic syndrome ocular anomalies (C536403)
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..Nephrotic Syndrome, Congenital, with or without Ocular Abnormalities (C563805)
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..Oculoauricular Syndrome (C567416)
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..Oculoauriculofrontonasal syndrome (C537865)
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..Oculocerebrocutaneous syndrome (C538088)
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..Oculodentodigital Dysplasia (C563160)
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..Oculodentodigital Dysplasia, Autosomal Recessive (C567605)
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..Oculomaxillofacial dysostosis (C537736)
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..Oculopalatocerebral Syndrome (C564935)
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..Oculopalatoskeletal syndrome (C537738)
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..Oculorenocerebellar syndrome (C537739)
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..Pena Shokeir syndrome Type 2 (C536646)
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..Persistent Hyperplastic Primary Vitreous (D054514)
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..Persistent Hyperplastic Primary Vitreous, Autosomal Recessive (C566966)
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..Peters anomaly (C537884)
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..PHACE association (C537892)
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..Pierson syndrome (C537185)
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..Popliteal Pterygium Syndrome (C562509)
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..Popliteal Pterygium Syndrome, Lethal Type (C564874)
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..Prepapillary Vascular Loops (C563287)
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..Pupil, Egg-Shaped (C566731)
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..Pupillary Membrane, Persistence Of (C562700)
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..Retinal Dysplasia (D015792) 2
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..Rieger syndrome 2 (C535680)
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..Rozin Hertz Goodman syndrome (C535876)
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..Torsion dystonia with onset in infancy (C536969)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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