Disease Browser
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Parent Node: Abnormalities, Multiple (D000015) | Parent Node: Agenesis of Corpus Callosum (D061085) | Parent Node: Macular Degeneration (D008268) | ..Starting node ..Stargardt Macular Degeneration Absent or Hypoplastic Corpus Callosum Mental Retardation and Dysmorphic Features (C548086)
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Sister Nodes: | ..Ectodermal dysplasia, ectrodactyly, and macular dystrophy (C536190)
| ..Fundus Dystrophy, Pseudoinflammatory, Of Sorsby (C564992)
| ..Geographic Atrophy (D057092)
| ..Juvenile macular degeneration and hypotrichosis (C537698)
| ..Macular Degeneration, Age-Related, 1 (C566411)
| ..Macular Degeneration, Age-Related, 10 (C566935)
| ..Macular Degeneration, Age-Related, 11 (C567450)
| ..Macular Degeneration, Age-Related, 2 (C562479)
| ..Macular Degeneration, Age-Related, 3 (C563838)
| ..Macular Degeneration, Age-Related, 4 (C565196)
| ..Macular Degeneration, Age-Related, 6 (C563674)
| ..Macular Degeneration, Age-Related, 7 (C565718)
| ..Macular Degeneration, Age-Related, 9 (C566958)
| ..Macular dystrophy, concentric annular (C537833)
| ..MACULAR DYSTROPHY, RETINAL, 3 (OMIM:608850)
| ..Macular Dystrophy, X-Linked (C564110)
| ..Macular Edema (D008269)
| ..Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders (C565786)
| ..OCCULT MACULAR DYSTROPHY (OMIM:613587)
| ..Stargardt disease 1 (C535804)
| ..Stargardt disease 3 (C535805)
| ..Stargardt disease 4 (C535521)
| ..Stargardt Macular Degeneration (C580470)
| ..Stargardt Macular Degeneration Absent or Hypoplastic Corpus Callosum Mental Retardation and Dysmorphic Features (C548086)
| ..Vitelliform Macular Dystrophy (D057826) 2
| ..Wet Macular Degeneration (D057135)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 10648 |
Name: | Stargardt Macular Degeneration Absent or Hypoplastic Corpus Callosum Mental Retardation and Dysmorphic Features |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D000015|MESH:D008268|MESH:D061085 |
TreeNumbers: | C10.500.034/C548086 |C11.768.585.439/C548086 |C16.131.077/C548086 |C16.131.666.034/C548086 |C23.300.008/C548086 |
Synonyms: | |
Slim Mappings: | Congenital abnormality|Eye disease|Nervous system disease|Pathology (anatomical condition) |
Reference: |
MedGen: C548086
MeSH: C548086
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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