Kallmann Syndrome [Kallmannův syndrom]

topical
10
Terms

autozomálně dominantní forma Kallmannova syndromu
hypogonadismus s anosmií
hypogonadotropní hypogonadismus a anosmie
hypogonadotropní hypogonadismus s anosmií
Kallmannův syndrom 1
Kallmannův syndrom 2
Kallmannův syndrom 3
olfaktogenitální syndrom
X-vázaná forma Kallmannova syndromu

 

Anosmic Hypogonadism
Anosmic Idiopathic Hypogonadotropic Hypogonadism
Autosomal Dominant Form of Kallmann Syndrome
Autosomal Recessive Form of Kallmann Syndrome
Dysplasia Olfactogenitalis of De Morsier
Hypogonadotropic Hypogonadism and Anosmia
Hypogonadotropic Hypogonadism-Anosmia Syndrome
Hypogonadotropic Hypogonadism, Anosmia, and Midline Cranial Anomalies (Cleft Lip, Cleft Palate and Imperfect Fusion)
Kallmann Syndrome 1
Kallmann Syndrome 2
Kallmann Syndrome 3
Kallmann Syndrome, Type 1, X-linked
Kallmann Syndrome, Type 3, Recessive
Kallmann's Syndrome

Persistent link   https://www.medvik.cz/link/D017436
Definition

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.

DUI
D017436 MeSH Browser
CUI
M0026453
Previous indexing
Hypogonadism (1966-1992)
History note
93
Public note
93

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications
DI
diagnosis 4
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy 2
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology 1
GE
genetics 1
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology
PP
physiopathology 1
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy 2
UR
urine
VE
veterinary
VI
virology

C Diseases
C12 Urogenital Diseases 8
C12.050 Female Urogenital Diseases and Pregnancy Complications 132
C12.050.351 Female Urogenital Diseases 153
C12.050.351.875 Urogenital Abnormalities 146
C12.050.351.875.253 Disorders of Sex Development 232
C12.050.351.875.253.096 Disorder of Sex Development, 46,XY 8
C12.050.351.875.253.096.500 Androgen-Insensitivity Syndrome 56
C12.050.351.875.253.096.562 Denys-Drash Syndrome 2
C12.050.351.875.253.096.624 Frasier Syndrome
C12.050.351.875.253.096.687 Gonadal Dysgenesis, 46,XY 22
C12.050.351.875.253.096.750 Kallmann Syndrome 10
C12.050.351.875.253.096.875 WAGR Syndrome 3
C12.200 Male Urogenital Diseases 200
C12.200.706 Urogenital Abnormalities 146
C12.200.706.316 Disorders of Sex Development 232
C12.200.706.316.096 Disorder of Sex Development, 46,XY 8
C12.200.706.316.096.500 Androgen-Insensitivity Syndrome 56
C12.200.706.316.096.562 Denys-Drash Syndrome 2
C12.200.706.316.096.624 Frasier Syndrome
C12.200.706.316.096.687 Gonadal Dysgenesis, 46,XY 22
C12.200.706.316.096.750 Kallmann Syndrome 10
C12.200.706.316.096.875 WAGR Syndrome 3
C12.800 Urogenital Abnormalities 146
C12.800.316 Disorders of Sex Development 232
C12.800.316.096 Disorder of Sex Development, 46,XY 8
C12.800.316.096.500 Androgen-Insensitivity Syndrome 56
C12.800.316.096.562 Denys-Drash Syndrome 2
C12.800.316.096.624 Frasier Syndrome
C12.800.316.096.687 Gonadal Dysgenesis, 46,XY 22
C12.800.316.096.750 Kallmann Syndrome 10
C12.800.316.096.875 WAGR Syndrome 3
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 753
C16.131.939 Urogenital Abnormalities 146
C16.131.939.316 Disorders of Sex Development 232
C16.131.939.316.096 Disorder of Sex Development, 46,XY 8
C16.131.939.316.096.500 Androgen-Insensitivity Syndrome 56
C16.131.939.316.096.562 Denys-Drash Syndrome 2
C16.131.939.316.096.624 Frasier Syndrome
C16.131.939.316.096.687 Gonadal Dysgenesis, 46,XY 22
C16.131.939.316.096.750 Kallmann Syndrome 10
C16.131.939.316.096.875 WAGR Syndrome 3
C16.320 Genetic Diseases, Inborn 1 215
C16.320.033 Adrenal Hyperplasia, Congenital 226
C16.320.051 Alagille Syndrome 19
C16.320.060 alpha 1-Antitrypsin Deficiency 86
C16.320.070 Anemia, Hemolytic, Congenital 48
C16.320.077 Anemia, Hypoplastic, Congenital 3
C16.320.080 Ataxia Telangiectasia 48
C16.320.089 Autoimmune Lymphoproliferative Syndrome 2
C16.320.099 Blood Coagulation Disorders, Inherited 64
C16.320.100 Brugada Syndrome 40
C16.320.129 CADASIL 8
C16.320.144 Camurati-Engelmann Syndrome 6
C16.320.160 Cardiomyopathy, Hypertrophic, Familial 33
C16.320.165 CHARGE Syndrome 1
C16.320.170 Cherubism 1
C16.320.180 Chromosome Disorders 260
C16.320.184 Ciliopathies 9
C16.320.188 Costello Syndrome 3
C16.320.190 Cystic Fibrosis 1 330
C16.320.215 Donohue Syndrome 1
C16.320.240 Dwarfism 99
C16.320.290 Eye Diseases, Hereditary 58
C16.320.298 Familial Multiple Lipomatosis
C16.320.306 Frasier Syndrome
C16.320.314 GATA2 Deficiency 2
C16.320.322 Genetic Diseases, X-Linked 60
C16.320.338 Genetic Diseases, Y-Linked 1
C16.320.355 Hajdu-Cheney Syndrome 6
C16.320.365 Hemoglobinopathies 68
C16.320.382 Hereditary Autoinflammatory Diseases 47
C16.320.400 Heredodegenerative Disorders, Nervous System 46
C16.320.413 Hyper-IgM Immunodeficiency Syndrome 4
C16.320.427 Hyperthyroxinemia, Familial Dysalbuminemic 2
C16.320.447 Imprinting Disorders
C16.320.467 Kallmann Syndrome 10
C16.320.480 Kartagener Syndrome 46
C16.320.488 Laminopathies 2
C16.320.495 Lennox Gastaut Syndrome 6
C16.320.510 Loeys-Dietz Syndrome 7
C16.320.540 Marfan Syndrome 105
C16.320.565 Metabolism, Inborn Errors 714
C16.320.577 Muscular Dystrophies 141
C16.320.590 Myasthenic Syndromes, Congenital 21
C16.320.600 Nail-Patella Syndrome 8
C16.320.700 Neoplastic Syndromes, Hereditary 144
C16.320.709 Oculocerebrorenal Syndrome 9
C16.320.714 Orofaciodigital Syndromes 7
C16.320.718 Osteoarthropathy, Primary Hypertrophic 127
C16.320.728 Osteochondrodysplasias 125
C16.320.737 Osteogenesis Imperfecta 106
C16.320.775 Pain Insensitivity, Congenital 10
C16.320.784 Pelger-Huet Anomaly 7
C16.320.798 Primary Immunodeficiency Diseases 48
C16.320.812 Pycnodysostosis 2
C16.320.831 Renal Tubular Transport, Inborn Errors 36
C16.320.850 Skin Diseases, Genetic 89
C16.320.925 Werner Syndrome 14
C16.320.962 Yellow Nail Syndrome
C19 Endocrine System Diseases 887
C19.391 Gonadal Disorders 40
C19.391.119 Disorders of Sex Development 232
C19.391.119.096 Disorder of Sex Development, 46,XY 8
C19.391.119.096.500 Androgen-Insensitivity Syndrome 56
C19.391.119.096.562 Denys-Drash Syndrome 2
C19.391.119.096.624 Frasier Syndrome
C19.391.119.096.687 Gonadal Dysgenesis, 46,XY 22
C19.391.119.096.750 Kallmann Syndrome 10
C19.391.119.096.875 WAGR Syndrome 3
C19.391.482 Hypogonadism 274
C19.391.482.293 Eunuchism 10
C19.391.482.600 Kallmann Syndrome 10
C19.391.482.629 Klinefelter Syndrome 82
C19.391.482.814 Sexual Infantilism 3

Brachytelephalangy characteristic facies Kallmann Disease MeSH Browser

Hypogonadotropic hypogonadism and anosmia, autosomal dominant Disease MeSH Browser

Kallmann Syndrome 2 with Bimanual Synkinesia Disease MeSH Browser

Kallmann Syndrome 2 with Cleft Lip or Palate Disease MeSH Browser

Kallmann Syndrome 2 with Selective Tooth Agenesis Disease MeSH Browser

Kallmann Syndrome 4 Disease MeSH Browser

Kallmann Syndrome 5 Disease MeSH Browser

Kallmann Syndrome 6 Disease MeSH Browser

Spastic paraplegia with Kallmann syndrome Disease MeSH Browser

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