loading...| Preferred Name | Charcot-Marie-Tooth Disease, Type IB | |
| Synonyms |
charcot mari tooth syndrom hereditary motor and sensory neuropathy 1b dystasias, hereditari areflex charcot marie tooth disease, type ia roussy-levi diseas charcot mari tooth disease, type i charcot mari tooth disease, type ib charcot mari tooth disease, type ii charcot mari tooth disease, type ia hereditary motor and sensory neuropathy ia hereditari motor and sensory-neuropathi type ii charcot-marie-tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1b hereditary areflexic dystasia charcot-marie-tooth syndrom areflexic dystasia, hereditari areflexic dystasia, hereditary atrophy, muscular, peron charcot-marie-tooth diseas charcot-marie-tooth disease hmsn type ii charcot mari tooth hereditari neuropathi roussi levi disea roussy-levi disea charcot-marie-tooth neuropathy, type 1a charcot-marie-tooth neuropathy, type 1b charcot-marie-tooth disease, type 1b muscular atrophies, peroneal muscular atrophy, peron charcot marie tooth diseas charcot marie tooth disease roussy-levy hereditary areflexic dystasia atrophy, peroneal muscular charcot marie tooth syndrome peroneal muscular atrophies charcot-marie diseas charcot-marie disease atrophies, peron muscular hereditari motor and sensori neuropathi type ii charcot-marie-tooth syndrome hereditari neuropathy, charcot-marie-tooth charcot-marie-tooth disease, autosom dominant, with focal fold myelin sheaths, type 1b charcot marie tooth disease, type ib neuropathy, type i hereditary motor and sensori neuropathy, type i hereditary motor and sensory roussy-levy syndrom charcot-marie-tooth disease, type ia hereditari motor and sensori neuropathi ia charcot marie tooth syndrom areflexic dystasias, hereditary areflexic dystasias, hereditari peron muscular atrophi roussy-levi syndrom roussy-levi hereditari areflex dystasia charcot marie tooth disease, type 1a atrophy, muscular, peroneal dystasia, hereditary areflex dystasia, hereditary areflexic dystasias, hereditary areflex hereditary type i motor and sensory neuropathi hereditari motor, and sensori neuropathi type i charcot mari tooth disea charcot mari tooth diseas charcot-marie-tooth disease, demyelinating, type 1a charcot-marie-tooth disease, demyelinating, type 1b charcot marie diseas charcot marie disease atrophies, peroneal muscular roussy levy syndrome roussy levy diseas roussy levy disease charcot mari tooth neuropathy, type 1b hereditary motor and sensory neuropathy 1a charcot-marie-tooth disease, type i hmsn type i hereditary motor and sensory neuropathy ib charcot-marie-tooth disease, type ii charcot marie tooth disease, type 1b roussy levy syndrom hereditary areflexic dystasias charcot-marie-tooth disease, slow nerv conduct type, link to duffi hereditary motor and sensory neuropathy type ii charcot-marie-tooth disease, autosom dominant, with focal fold myelin sheaths, type 1a neuropathy, type ii hereditari motor and sensori hmn distal type i roussi levi diseas charcot-marie-tooth disease, slow nerve conduction type, linked to duffi charcot-marie-tooth disease, type ib charcot mari tooth disease, type 1a charcot mari tooth disease, type 1b peroneal muscular atrophi peroneal muscular atrophy muscular atrophies, peron charcot-marie-tooth disease, type 1a roussi levi hereditari areflex dystasia dystasia, hereditari areflex hereditari areflex dystasia charcot-marie-tooth hereditari neuropathi charcot mari tooth neuropathy, type 1a atrophy, peron muscular hereditari motor and sensori neuropathi 1a neuropathy, type ii hereditary motor and sensori hereditary neuropathy, charcot-marie-tooth hereditari type i motor and sensori neuropathi roussy levy hereditary areflexic dystasia roussy-levy diseas roussy-levy disease neuropathy, type ii hereditary motor and sensory charcot marie tooth disease, type ii neuropathy, type i hereditari motor and sensori roussi levi syndrom hereditary type i motor and sensory neuropathy hereditary motor and sensory-neuropathy type ii charcot marie tooth neuropathy, type 1a charcot marie tooth neuropathy, type 1b charcot-marie-tooth disea syndrome, charcot-marie-tooth muscular atrophy, peroneal roussy-levy syndrome charcot marie tooth disease, type i charcot-marie-tooth disease, slow nerve conduction type, linked to duffy areflex dystasias, hereditari charcot mari disea charcot mari diseas charcot marie tooth hereditary neuropathy charcot marie tooth hereditary neuropathi dystasias, hereditary areflexic charcot-marie-tooth hereditary neuropathy charcot-marie-tooth hereditary neuropathi areflex dystasia, hereditari hereditari motor and sensori neuropathi ib charcot-marie-tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1a charcot-mari disea charcot-mari diseas hereditary motor, and sensory neuropathy type i hereditari motor and sensori neuropathi 1b syndrome, roussy-levi syndrome, roussy-levy charcot- marie- tooth disease, type i b hmsn 1a hmsn 1b hmsn i hmsn ia hmsn ib hmsn ii hmsn1a hmsn1b |
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| ID |
http://id.nlm.nih.gov/mesh/D002607 |
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charcot mari tooth syndrom hereditary motor and sensory neuropathy 1b dystasias, hereditari areflex charcot marie tooth disease, type ia roussy-levi diseas charcot mari tooth disease, type i charcot mari tooth disease, type ib charcot mari tooth disease, type ii charcot mari tooth disease, type ia hereditary motor and sensory neuropathy ia hereditari motor and sensory-neuropathi type ii charcot-marie-tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1b hereditary areflexic dystasia charcot-marie-tooth syndrom areflexic dystasia, hereditari areflexic dystasia, hereditary atrophy, muscular, peron charcot-marie-tooth diseas charcot-marie-tooth disease hmsn type ii charcot mari tooth hereditari neuropathi roussi levi disea roussy-levi disea charcot-marie-tooth neuropathy, type 1a charcot-marie-tooth neuropathy, type 1b charcot-marie-tooth disease, type 1b muscular atrophies, peroneal muscular atrophy, peron charcot marie tooth diseas charcot marie tooth disease roussy-levy hereditary areflexic dystasia atrophy, peroneal muscular charcot marie tooth syndrome peroneal muscular atrophies charcot-marie diseas charcot-marie disease atrophies, peron muscular hereditari motor and sensori neuropathi type ii charcot-marie-tooth syndrome hereditari neuropathy, charcot-marie-tooth charcot-marie-tooth disease, autosom dominant, with focal fold myelin sheaths, type 1b charcot marie tooth disease, type ib neuropathy, type i hereditary motor and sensori neuropathy, type i hereditary motor and sensory roussy-levy syndrom charcot-marie-tooth disease, type ia hereditari motor and sensori neuropathi ia charcot marie tooth syndrom areflexic dystasias, hereditary areflexic dystasias, hereditari peron muscular atrophi roussy-levi syndrom roussy-levi hereditari areflex dystasia charcot marie tooth disease, type 1a atrophy, muscular, peroneal dystasia, hereditary areflex dystasia, hereditary areflexic dystasias, hereditary areflex hereditary type i motor and sensory neuropathi hereditari motor, and sensori neuropathi type i charcot mari tooth disea charcot mari tooth diseas charcot-marie-tooth disease, demyelinating, type 1a charcot-marie-tooth disease, demyelinating, type 1b charcot marie diseas charcot marie disease atrophies, peroneal muscular roussy levy syndrome roussy levy diseas roussy levy disease charcot mari tooth neuropathy, type 1b hereditary motor and sensory neuropathy 1a charcot-marie-tooth disease, type i hmsn type i hereditary motor and sensory neuropathy ib charcot-marie-tooth disease, type ii charcot marie tooth disease, type 1b roussy levy syndrom hereditary areflexic dystasias charcot-marie-tooth disease, slow nerv conduct type, link to duffi hereditary motor and sensory neuropathy type ii charcot-marie-tooth disease, autosom dominant, with focal fold myelin sheaths, type 1a neuropathy, type ii hereditari motor and sensori hmn distal type i roussi levi diseas charcot-marie-tooth disease, slow nerve conduction type, linked to duffi charcot-marie-tooth disease, type ib charcot mari tooth disease, type 1a charcot mari tooth disease, type 1b peroneal muscular atrophi peroneal muscular atrophy muscular atrophies, peron charcot-marie-tooth disease, type 1a roussi levi hereditari areflex dystasia dystasia, hereditari areflex hereditari areflex dystasia charcot-marie-tooth hereditari neuropathi charcot mari tooth neuropathy, type 1a atrophy, peron muscular hereditari motor and sensori neuropathi 1a neuropathy, type ii hereditary motor and sensori hereditary neuropathy, charcot-marie-tooth hereditari type i motor and sensori neuropathi roussy levy hereditary areflexic dystasia roussy-levy diseas roussy-levy disease neuropathy, type ii hereditary motor and sensory charcot marie tooth disease, type ii neuropathy, type i hereditari motor and sensori roussi levi syndrom hereditary type i motor and sensory neuropathy hereditary motor and sensory-neuropathy type ii charcot marie tooth neuropathy, type 1a charcot marie tooth neuropathy, type 1b charcot-marie-tooth disea syndrome, charcot-marie-tooth muscular atrophy, peroneal roussy-levy syndrome charcot marie tooth disease, type i charcot-marie-tooth disease, slow nerve conduction type, linked to duffy areflex dystasias, hereditari charcot mari disea charcot mari diseas charcot marie tooth hereditary neuropathy charcot marie tooth hereditary neuropathi dystasias, hereditary areflexic charcot-marie-tooth hereditary neuropathy charcot-marie-tooth hereditary neuropathi areflex dystasia, hereditari hereditari motor and sensori neuropathi ib charcot-marie-tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1a charcot-mari disea charcot-mari diseas hereditary motor, and sensory neuropathy type i hereditari motor and sensori neuropathi 1b syndrome, roussy-levi syndrome, roussy-levy charcot- marie- tooth disease, type i b hmsn 1a hmsn 1b hmsn i hmsn ia hmsn ib hmsn ii hmsn1a hmsn1b |
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| label |
Charcot-Marie-Tooth Disease, Type IB |
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| prefixIRI |
MeSH:D002607 |
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| prefLabel |
Charcot-Marie-Tooth Disease, Type IB |
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| Delete | Mapping To | Ontology | Source |
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| http://purl.bioontology.org/ontology/SNOMEDCT/42986003 | SNOMEDCT | LOOM | |
| http://purl.bioontology.org/ontology/SNMI/DA-44023 | SNMI | LOOM |