Dwarfism [nanismus]

topical
99
Terms

Nanism

Persistent link   https://www.medvik.cz/link/D004392
Definition

A genetic or pathological condition that is characterized by short stature and undersize. Abnormal skeletal growth usually results in an adult who is significantly below the average height.

DUI
D004392 MeSH Browser
CUI
M0006897

C Diseases
C05.116 Bone Diseases 796
C05.116.099.052 Acro-Osteolysis 3
C05.116.099.105 Basal Cell Nevus Syndrome 33
C05.116.099.343 Dwarfism 99
C05.116.099.343.110 Achondroplasia 71
C05.116.099.343.250 Cockayne Syndrome 4
C05.116.099.343.347 Congenital Hypothyroidism 151
C05.116.099.343.445 Dwarfism, Pituitary 50
C05.116.099.343.679 Laron Syndrome 1
C05.116.099.343.796 Mulibrey Nanism 1
C05.116.099.343.957 Weill-Marchesani Syndrome 1
C05.116.099.370 Dysostoses 22
C05.116.099.386 Funnel Chest 38
C05.116.099.492 Gigantism 14
C05.116.099.655 Leg Length Inequality 118
C05.116.099.674 Marfan Syndrome 105
C05.116.099.708 Osteochondrodysplasias 125
C05.116.099.736 Osteolysis, Essential 8
C05.116.099.739 Pectus Carinatum 1
C05.116.099.742 Platybasia 12
C05.116.099.750 Proteus Syndrome 8
C16.320.051 Alagille Syndrome 19
C16.320.100 Brugada Syndrome 40
C16.320.129 CADASIL 8
C16.320.165 CHARGE Syndrome 1
C16.320.170 Cherubism 1
C16.320.180 Chromosome Disorders 259
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
C16.320.240.500 Achondroplasia 71
C16.320.240.562 Cockayne Syndrome 4
C16.320.240.625 Congenital Hypothyroidism 151
C16.320.240.750 Laron Syndrome 1
C16.320.240.875 Mulibrey Nanism 1
C16.320.240.937 Silver-Russell Syndrome 3
C16.320.306 Frasier Syndrome
C16.320.314 GATA2 Deficiency 2
C16.320.365 Hemoglobinopathies 68
C16.320.467 Kallmann Syndrome 10
C16.320.480 Kartagener Syndrome 46
C16.320.488 Laminopathies 2
C16.320.540 Marfan Syndrome 105
C16.320.577 Muscular Dystrophies 140
C16.320.728 Osteochondrodysplasias 125
C16.320.784 Pelger-Huet Anomaly 7
C16.320.812 Pycnodysostosis 2
C16.320.925 Werner Syndrome 14
C19.246 Diabetes Mellitus 9 559
C19.297 Dwarfism 99
C19.297.312 Dwarfism, Pituitary 50
C19.297.656 Laron Syndrome 1
C19.874 Thyroid Diseases 1 307

Aarskog Syndrome Disease MeSH Browser

Abuse dwarfism syndrome Disease MeSH Browser

Acromesomelic dysplasia Disease MeSH Browser

Acromesomelic dysplasia Campailla-Martinelli type Disease MeSH Browser

Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus Disease MeSH Browser

Alopecia contractures dwarfism mental retardation Disease MeSH Browser

Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis Disease MeSH Browser

Anauxetic dysplasia Disease MeSH Browser

Astley-Kendall syndrome Disease MeSH Browser

Asymmetric Short Stature Syndrome Disease MeSH Browser

Bangstad syndrome Disease MeSH Browser

Bird headed dwarfism Montreal type Disease MeSH Browser

Boomerang dysplasia Disease MeSH Browser

Brachydactylous dwarfism Mseleni type Disease MeSH Browser

Brachymetapody-Anodontia-Hypotrichosis-Albinoidism Disease MeSH Browser

Brunoni syndrome Disease MeSH Browser

Bullous Dystrophy, Hereditary Macular Type Disease MeSH Browser

Cantu Sanchez-Corona Fragoso syndrome Disease MeSH Browser

Chondrodysplasia Calcificans Metaphysealis Disease MeSH Browser

Chondrodysplasia, Megarbane-Dagher-Melki Type Disease MeSH Browser

De Sanctis-Cacchione syndrome Disease MeSH Browser

Desbuquois syndrome Disease MeSH Browser

Diastrophic Dysplasia, Broad Bone-Platyspondylic Variant Disease MeSH Browser

Diastrophic dysplasia Disease MeSH Browser

Disproportionate Short Stature with Ptosis and Valvular Heart Lesions Disease MeSH Browser

Dwarfism stiff joint ocular abnormalities Disease MeSH Browser

Dwarfism tall vertebrae Disease MeSH Browser

Dwarfism, Familial, With Muscle Spasms Disease MeSH Browser

Dwarfism, Levi Type Disease MeSH Browser

Dwarfism, Low-Birth-Weight Type, with Unresponsiveness to Growth Hormone Disease MeSH Browser

Dwarfism, Proportionate, with Hip Dislocation Disease MeSH Browser

Dyggve-Melchior-Clausen syndrome Disease MeSH Browser

Dyssegmental Dysplasia with Glaucoma Disease MeSH Browser

Dyssegmental dysplasia Disease MeSH Browser

Fibrochondrogenesis Disease MeSH Browser

Gerodermia osteodysplastica Disease MeSH Browser

Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Disease MeSH Browser

Hadziselimovic Syndrome Disease MeSH Browser

Hypochondroplasia Disease MeSH Browser

Ichthyosis, mental retardation, dwarfism, and renal impairment Disease MeSH Browser

Isolated Growth Hormone Deficiency, Type IB Disease MeSH Browser

Kenny-Caffey syndrome, type 2 Disease MeSH Browser

Keratosis follicularis dwarfism cerebral atrophy Disease MeSH Browser

Kniest dysplasia Disease MeSH Browser

Laplane Fontaine Lagardere syndrome Disease MeSH Browser

Megaepiphyseal dwarfism Disease MeSH Browser

Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations Disease MeSH Browser

Mental retardation, macrocephaly, short stature and craniofacial dysmorphism Disease MeSH Browser

Mesomelic Dwarfism of Hypoplastic Tibia and Radius Type Disease MeSH Browser

Mesomelic dwarfism Reinhardt Pfeiffer type Disease MeSH Browser

Metatropic Dwarfism, Type II Disease MeSH Browser

Metatropic dwarfism Disease MeSH Browser

Microcephalic Osteodysplastic Primordial Dwarfism, Type II Disease MeSH Browser

Microcephalic osteodysplastic primordial dwarfism, type 1 Disease MeSH Browser

Microcephalic osteodysplastic primordial dwarfism, type 3 Disease MeSH Browser

Microcephalic primordial dwarfism Toriello type Disease MeSH Browser

Miller-McKusick-Malvaux-Syndrome (3M Syndrome) Disease MeSH Browser

Mollica Pavone Antener syndrome Disease MeSH Browser

Nievergelt syndrome Disease MeSH Browser

Oculopalatocerebral Syndrome Disease MeSH Browser

Oliver-McFarlane syndrome Disease MeSH Browser

Parastremmatic dwarfism Disease MeSH Browser

Pseudodiastrophic dysplasia Disease MeSH Browser

Rapadilino syndrome Disease MeSH Browser

Robinow Syndrome Disease MeSH Browser

Rommen Mueller Sybert syndrome Disease MeSH Browser

Ruvalcaba Syndrome Disease MeSH Browser

Seckel Syndrome 3 Disease MeSH Browser

Seckel like syndrome type Buebel Disease MeSH Browser

Seckel syndrome 1 Disease MeSH Browser

Seckel syndrome 2 Disease MeSH Browser

Short Stature And Facioauriculothoracic Malformations Disease MeSH Browser

Short Stature, Mental Retardation, Callosal Agenesis, Heminasal Hypoplasia, Microphthalmia, And Atypical Clefting Disease MeSH Browser

Short Stature-Obesity Syndrome Disease MeSH Browser

Short limb dwarfism Al Gazali type Disease MeSH Browser

Singh Chhaparwal Dhanda syndrome Disease MeSH Browser

Spondyloepiphyseal dysplasia tarda, Toledo type Disease MeSH Browser

Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type Disease MeSH Browser

Synovial Chondromatosis, Familial, with Dwarfism Disease MeSH Browser

Thoraco limb dysplasia Rivera type Disease MeSH Browser

Thoracomelic Dysplasia Disease MeSH Browser

Three M Syndrome 2 Disease MeSH Browser

Tryptophanuria With Dwarfism Disease MeSH Browser

Weill-Marchesani-Like Syndrome Disease MeSH Browser