Disease Browser
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Parent Node:
Abnormalities, Multiple (D000015) | Parent Node:
Cataract (D002386) | Parent Node:
Corneal Dystrophies, Hereditary (D003317) | Parent Node:
Myopia (D009216) | Parent Node:
Spinocerebellar Degenerations (D013132) | ..Starting node .. Mousa Al din Al Nassar syndrome (C536989)
| Child Nodes:
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Sister Nodes: | .. Corneal cerebellar syndrome (C535472)
| .. Friedreich Ataxia (D005621) 6 C:1
| .. Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy (C564264)
| .. Hereditary spinal ataxia (C531684)
| .. Infantile onset spinocerebellar ataxia (C535523) 1 C:1
| .. LICHTENSTEIN-KNORR SYNDROME (OMIM:616291)
| .. Mousa Al din Al Nassar syndrome (C536989)
| .. Myoclonic Cerebellar Dyssynergia (D002527) 1
| .. Olivopontocerebellar Atrophies (D009849) 15 C:1
| .. Posterior column ataxia (C536342)
| .. Sensorimotor neuropathy with ataxia, autosomal dominant (C537197)
| .. Spinocerebellar ataxia 19 (C537198)
| .. Spinocerebellar ataxia 21 (C537200)
| .. Spinocerebellar ataxia 22 (C542540)
| .. Spinocerebellar ataxia 23 (C537201)
| .. Spinocerebellar ataxia 27 (C537204)
| .. Spinocerebellar Ataxia 29 (C537206)
| .. Spinocerebellar ataxia 8 (C537307)
| .. Spinocerebellar Ataxia, Autosomal Recessive 2 (C565865)
| .. Spinocerebellar ataxia, autosomal recessive 3 (C537309)
| .. Spinocerebellar ataxia, autosomal recessive 4 (C537310)
| .. Spinocerebellar ataxia, autosomal recessive 5 (C537311)
| .. Spinocerebellar ataxia, autosomal recessive 6 (C537312)
| .. Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy (C537313)
| .. Spinocerebellar ataxia, X-linked, 2 (C537314)
| .. Spinocerebellar ataxia, X-linked, 4 (C537316)
| .. Spinocerebellar Ataxias (D020754) 34 C:2
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD
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Term ID: | 8187 |
Name: | Mousa Al din Al Nassar syndrome |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D000015|MESH:D002386|MESH:D003317|MESH:D009216|MESH:D013132 |
TreeNumbers: | C10.228.140.252.700/C536989 |C10.228.854.787/C536989 |C10.574.500.825/C536989 |C11.204.236/C536989 |C11.270.162/C536989 |C11.510.245/C536989 |C11.744.636/C536989 |C16.131.077/C536989 |C16.320.290.162/C536989 |C16.320.400.780/C536989 |
Synonyms: | Bedouin spastic ataxia syndrome |
Slim Mappings: | Congenital abnormality|Eye disease|Genetic disease (inborn)|Nervous system disease |
Reference: |
MedGen: C536989
MeSH: C536989
OMIM: MSeqDR : Genes: | Phenotypes | | Disease Causing ClinVar Variants | | MSeqDR Portal | |
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