Search on: KALLMANN SYNDROME 
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Descriptor English:   Kallmann Syndrome 
Descriptor Spanish:   Síndrome de Kallmann 
Descriptor Portuguese:   Síndrome de Kallmann 
Tree Number:   C12.706.842.425
C13.351.875.842.425
C16.131.939.842.425
C16.320.467
C19.391.482.600
C19.391.775.425
Definition English:   A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait. 
History Note English:   93 
Allowable Qualifiers English:  
blood cerebrospinal fluid
chemically induced classification
congenital complications
diet therapy diagnosis
drug therapy economics
ethnology embryology
enzymology epidemiology
etiology genetics
history immunology
metabolism microbiology
mortality nursing
pathology prevention & control
physiopathology parasitology
psychology radiography
rehabilitation radionuclide imaging
radiotherapy surgery
therapy urine
ultrasonography veterinary
virology  
Record Number:   30678 
Unique Identifier:   D017436 

Occurrence in VHL:
 

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