Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandAbnormalities, Multiple (D000015)
Parent Node:
expandCataract (D002386)
Parent Node:
expandCorneal Dystrophies, Hereditary (D003317)
Parent Node:
expandMyopia (D009216)
Parent Node:
expandSpinocerebellar Degenerations (D013132)
..Starting node
..expandMousa Al din Al Nassar syndrome (C536989)

       Child Nodes:



 Sister Nodes: 
..expandCorneal cerebellar syndrome (C535472)
..expandFriedreich Ataxia (D005621) Child6
..expandGrowth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy (C564264)
..expandHereditary spinal ataxia (C531684)
..expandInfantile onset spinocerebellar ataxia (C535523) Child1
..expandMousa Al din Al Nassar syndrome (C536989)
..expandMyoclonic Cerebellar Dyssynergia (D002527) Child1
..expandOlivopontocerebellar Atrophies (D009849) Child15
..expandPosterior column ataxia (C536342)
..expandSensorimotor neuropathy with ataxia, autosomal dominant (C537197)
..expandSpinocerebellar ataxia 13 (C537195)
..expandSpinocerebellar ataxia 14 (C537196)
..expandSpinocerebellar ataxia 19 (C537198)
..expandSpinocerebellar ataxia 21 (C537200)
..expandSpinocerebellar ataxia 22 (C542540)
..expandSpinocerebellar ataxia 23 (C537201)
..expandSpinocerebellar ataxia 27 (C537204)
..expandSpinocerebellar ataxia 28 (C537205)
..expandSpinocerebellar Ataxia 29 (C537206)
..expandSpinocerebellar ataxia 8 (C537307)
..expandSpinocerebellar ataxia, autosomal recessive 1 (C537308)
..expandSpinocerebellar Ataxia, Autosomal Recessive 2 (C565865)
..expandSpinocerebellar ataxia, autosomal recessive 3 (C537309)
..expandSpinocerebellar ataxia, autosomal recessive 4 (C537310)
..expandSpinocerebellar ataxia, autosomal recessive 5 (C537311)
..expandSpinocerebellar ataxia, autosomal recessive 6 (C537312)
..expandSpinocerebellar ataxia, autosomal recessive, with axonal neuropathy (C537313)
..expandSpinocerebellar ataxia, X-linked, 2 (C537314)
..expandSpinocerebellar ataxia, X-linked, 4 (C537316)
..expandSpinocerebellar Ataxias (D020754) Child34
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:7399
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:

Genes:
Phenotypes
Disease Causing ClinVar Variants