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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Paralysis (D010243)
Parent Node: Respiratory Insufficiency (D012131)
..Starting node ..Respiratory Paralysis (D012133)
Child Nodes:
Sister Nodes:
..Acidosis, Respiratory (D000142)
..Airway Obstruction (D000402) 1
..Asphyxiating Thoracic Dystrophy 3 (C567761) 1
..Circumvallate Placenta Syndrome (C565847)
..Granuloma, Laryngeal (D006102)
..Hantavirus Pulmonary Syndrome (D018804)
..Hereditary Myopathy with Early Respiratory Failure (C566343)
..Hypoventilation (D007040) 3
..Infantile Apparent Life-Threatening Event (D057768)
..Positive-Pressure Respiration, Intrinsic (D018467)
..Respiratory Paralysis (D012133)
..Respiratory Underresponsiveness to Hypoxia and Hypercapnia (C564848)
..Tauopathy and Respiratory Failure (C563580)
..Thompson Baraitser syndrome (C536515)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9688
Name:	Respiratory Paralysis
Definition:	Complete or severe weakness of the muscles of respiration. This condition may be associated with MOTOR NEURON DISEASES; PERIPHERAL NERVE DISEASES; NEUROMUSCULAR JUNCTION DISEASES; SPINAL CORD DISEASES; injury to the PHRENIC NERVE; and other disorders.
Alternative IDs:
ParentIDs:	MESH:D010243\|MESH:D012131
TreeNumbers:	C08.618.846.812 \|C10.597.622.812 \|C23.888.592.636.812
Synonyms:	Diaphragmatic Paralysis \|Muscle Paralyses, Respiratory \|Muscle Paralysis, Respiratory \|Paralysis, Diaphragmatic \|Paralysis, Respiratory \|Paralysis, Respiratory Muscle \|Respiratory Muscle Paralysis
Slim Mappings:	Nervous system disease\|Respiratory tract disease\|Signs and symptoms
Reference:	MedGen: D012133 MeSH: D012133 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants