| Disease Browser
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Parent Node:
 Neuromuscular Manifestations (D020879) | ..Starting node
.. Muscle Hypotonia (D009123)
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Child Nodes:
| | ........Allan-Herndon-Dudley syndrome (C537047) | | ........Atonic-Astatic Syndrome of Foerster (C565926) | | ........Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities (C566234) | | ........Birk-Barel Mental Retardation Dysmorphism Syndrome (C567357) | | ........Carnitine Acetyltransferase Deficiency (C563249) | | ........Cohen syndrome (C536438) | | ........Combined Oxidative Phosphorylation Deficiency 3 (C566467) | | ........Creases, Infra-Auricular Cutaneous, with Tall Stature and Advanced Bone Age (C566543) | | ........Der Kaloustian Mcintosh Silver syndrome (C538217) | | ........Emanuel syndrome (C535733) | | ........Ethanolaminosis (C562651) | | ........Fumaric aciduria (C538191) | | ........German Syndrome (C562543) | | ........Grubben de Cock Borghgraef syndrome (C537621) | | ........Hydronephrosis, Congenital, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental Retardation (C565736) | | ........Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem response (C537159) | | ........Hypotonia, Seizures, And Precocious Puberty (C567566) | | ........Hypotonia-Cystinuria Syndrome (C564710) | | ........Joubert Syndrome 10 (C567582) | | ........Joubert syndrome 3 (C536295) | | ........Joubert syndrome 5 (C537688) | | ........Ketoadipicaciduria (C565453) | | ........MENTAL RETARDATION, AUTOSOMAL DOMINANT 20 (OMIM:613443) | | ........Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia (C563896) | | ........Miller-McKusick-Malvaux-Syndrome (3M Syndrome) (C535314) | | ........Opitz-Kaveggia syndrome (C537923) | | ........Qazi Markouizos syndrome (C536259) | | ........Radioulnar Synostosis, Unilateral, with Developmental Retardation and Hypotonia (C564856) | | ........Scalp ear nipple syndrome (C536623) | | ........Three M Syndrome 2 (C567862) |
Sister Nodes: | ..Fasciculation (D005207)  1
| ..Muscle Cramp (D009120) 3
| ..Muscle Hypertonia (D009122) 24
| ..Muscle Hypotonia (D009123) 30
| ..Muscle Weakness (D018908) 5
| ..Muscular Atrophy (D009133) 16
| ..Myokymia (D020385) 5
| ..Myotonia (D009222) 2
| ..Spasm (D013035) 8
| ..Tetany (D013746)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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| Term ID: | 7492 |
| Name: | Muscle Hypotonia |
| Definition: | A diminution of the skeletal muscle tone marked by a diminished resistance to passive stretching. |
| Alternative IDs: | |
| ParentIDs: | MESH:D020879 |
| TreeNumbers: | C10.597.613.575 |C23.888.592.608.575 |
| Synonyms: | Decreased Muscle Tone |Flaccidity, Muscle |Flaccidity, Muscular |Flaccid Muscle Tone |Floppy Muscle |Floppy Muscles |Hypomyotonia |Hypotonia |Hypotonia, Muscle |Hypotonia, Muscular |Hypotonia, Neonatal |Hypotonias, Neonatal |Hypotonias, Unilateral |Hypotonia, Unilate |
| Slim Mappings: | Nervous system disease|Signs and symptoms |
| Reference: |
MedGen: D009123
MeSH: D009123
OMIM:
Genes: | | Phenotypes | | | Disease Causing ClinVar Variants | |
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