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D017436

We use MeSH codes primarily for indexing, cataloging, and searching biomedical literature.
MSH Medical Subject Headings The original, English version of the vocabulary.
MSHPOR Portuguese Portuguese MeSH headings.
MSHSPA Spanish (Decs) Spanish MeSH headings (often referenced as DeCS—Descriptors in Health Sciences).
MSHRUS Russian Russian MeSH headings.
MSHITA Italian Italian MeSH headings.
MSHGER German German MeSH headings.
MSHFRE French French MeSH headings.
MSHSWE Swedish Swedish MeSH headings.
MSHCZE Czech Czech MeSH headings.
MSHFIN Finnish Finnish MeSH headings.
MSHJPN Japanese Japanese MeSH headings.
MSHLAV Latvian Latvian MeSH headings.
MSHSCR Serbo-Croatian Serbo-Croatian MeSH headings.
MSHPOL Polish Polish MeSH headings.
MSHNOR Norwegian Norwegian MeSH headings.
MSHDUT Dutch Dutch MeSH headings.


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Dict Code CUI Term Tree
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MSH D017436 C0162809 Syndrome, Kallmann's preferred
MSH D017436 C0162809 Kallmann Syndrome preferred
MSH D017436 C0162809 Kallmanns Syndrome preferred
MSH D017436 C0162809 Syndrome, Kallmann preferred
MSHSWE D017436 C0162809 Kallmanns syndrom preferred
MSHCZE D017436 C0162809 Kallmannův syndrom preferred
MSHFIN D017436 C0162809 Kallmannin oireyhtymä preferred
MSHRUS D017436 C0162809 KALLMENA SINDROM no pref
MSHJPN D017436 C0162809 Kallmann症候群 preferred
MSHPOL D017436 C0162809 Zespół węchowo-płciowy no pref
MSHPOL D017436 C0162809 Zespół Kallmanna preferred
MSH D017436 C0162809 Hypogonadism, Anosmic no pref
MSH D017436 C0162809 Hypogonadisms, Anosmic no pref
MSH D017436 C0162809 Anosmic Hypogonadisms no pref
MSHNOR D017436 C0162809 Kallmanns syndrom preferred
MSH D017436 C0162809 Hypogonadotropic Hypogonadism and Anosmia no pref
MSH D017436 C0162809 Kallmann's Syndrome preferred
MSH D017436 C0162809 Hypogonadotropic Hypogonadism-Anosmia Syndrome no pref
MSH D017436 C0162809 Dysplasia Olfactogenitalis of De Morsier no pref
MSH D017436 C0162809 Anosmic Idiopathic Hypogonadotropic Hypogonadism no pref
MSH D017436 C0162809 Anosmic Hypogonadism no pref
MSHFRE D017436 C0162809 Dysplasie olfacto-génitale de De Morsier no pref
MSHFRE D017436 C0162809 Dysplasie olfactogénitale de De Morsier no pref
MSHFRE D017436 C0162809 Syndrome de Kallman-De Morsier no pref
MSHFRE D017436 C0162809 Dysplasie olfacto-génitale de Kallmann-De Morsier no pref
MSHCZE D017436 C0162809 hypogonadismus s anosmií no pref
MSHFRE D017436 C0162809 Syndrome de De Morsier-Kallmann no pref
MSHCZE D017436 C0162809 olfaktogenitální syndrom no pref
MSHFRE D017436 C0162809 Dysplasie olfactogénitale de Kallmann-De Morsier no pref
MSHNOR D017436 C0162809 Hypogonadotropisk eunukoidisme no pref
MSHCZE D017436 C0162809 hypogonadotropní hypogonadismus s anosmií no pref
MSHCZE D017436 C0162809 hypogonadotropní hypogonadismus a anosmie no pref
MSHFRE D017436 C0162809 Syndrome de Kallmann preferred
MSHGER D017436 C0162809 Kallmann-Syndrom preferred
MSHITA D017436 C0162809 Sindrome di Kallmann preferred
MSHJPN D017436 C0162809 カルマン症候群 no pref
MSHJPN D017436 C0162809 無嗅覚性性機能不全 no pref
MSHJPN D017436 C0162809 無嗅覚性性機能不全症 no pref
MSHJPN D017436 C0162809 無嗅覚性性機能低下 no pref
MSHJPN D017436 C0162809 無嗅覚性性機能低下症 no pref
MSHRUS D017436 C0162809 КАЛЛМЕНА СИНДРОМ preferred
MSHDUT D017436 C0162809 Kallmann-syndroom no pref
MSHDUT D017436 C0162809 Syndroom, Kallmann- preferred
MSHPOR D017436 C0162809 Síndrome de Kallmann preferred
MSHSPA D017436 C0162809 Síndrome de Kallmann no pref
MSHFRE D017436 C1563719 Syndrome de Kallmann de type 1 preferred
MSHCZE D017436 C1563719 Kallmannův syndrom 1 preferred
MSHNOR D017436 C1563719 Kallmanns syndrom type 1, X-bundet preferred
MSH D017436 C1563719 Kallmann Syndrome 1 preferred
MSH D017436 C1563719 Kallmann Syndrome, Type 1, X-linked no pref
MSHFRE D017436 C1563719 Syndrome de Kallmann de type I no pref
MSHCZE D017436 C1563719 X-vázaná forma Kallmannova syndromu no pref
MSHFRE D017436 C1563720 Syndrome de Kallmann de type 2 preferred
MSHCZE D017436 C1563720 Kallmannův syndrom 2 preferred
MSHNOR D017436 C1563720 Autosomalt dominant Kallmanns syndrom preferred
MSH D017436 C1563720 Kallmann Syndrome 2 preferred
MSH D017436 C1563720 Autosomal Dominant Form of Kallmann Syndrome no pref
MSHFRE D017436 C1563720 Syndrome de Kallmann de type II no pref
MSHCZE D017436 C1563720 autozomálně dominantní forma Kallmannova syndromu no pref
MSHCZE D017436 C2930927 Kallmannův syndrom 3 preferred
MSHNOR D017436 C2930927 Autosomalt recessivt Kallmanns syndrom preferred
MSH D017436 C2930927 Kallmann Syndrome, Type 3, Recessive preferred
MSH D017436 C2930927 Hypogonadotropic Hypogonadism, Anosmia, and Midline Cranial Anomalies (Cleft Lip, Cleft Palate and Imperfect Fusion) no pref
MSH D017436 C2930927 Autosomal Recessive Form of Kallmann Syndrome no pref
MSH D017436 C2930927 Kallmann Syndrome 3 no pref
D017436








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