Cyanosis
Symptom Information:
| Symptom ID: | HPO:0000961 | ||||
| Synonyms: |
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| Quality: | |||||
| Cross references: |
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| Is a (Direct Parents): |
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| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Generalized abnormality of skin(HPO:0011354) Dermatological manifestations of systemic disorders(HPO:0001005) Cyanosis(HPO:0000961) Abnormality of the respiratory system(HPO:0002086) Functional respiratory abnormality(HPO:0002795) Cyanosis(HPO:0000961) MedDRA: |
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| Database Frequency: | 60 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| APNEA, CENTRAL SLEEP | (OMIM:207720) |
| ATRIOVENTRICULAR SEPTAL DEFECT 3 | (OMIM:600309) |
| Acute interstitial pneumonia | (Orphanet:79126) |
| Alström syndrome | (Orphanet:64) |
| Arnold-Chiari malformation type II | (Orphanet:1136) |
| Arterial calcification, generalized, of infancy, 1 | (OMIM:208000) |
| Atrioventricular canal defect | (Orphanet:98722) |
| BREATH-HOLDING SPELLS | (OMIM:607578) |
| Benign familial infantile seizures | (Orphanet:306) |
| Benign familial neonatal-infantile seizures | (Orphanet:140927) |
| CHOLESTEROL PNEUMONIA | (OMIM:215030) |
| CREST syndrome | (Orphanet:90290) |
| CYANOSIS AND HEPATIC DISEASE | (OMIM:219400) |
| Cardiomyopathy-hypotonia-lactic acidosis syndrome | (Orphanet:91130) |
| Chronic respiratory distress with surfactant metabolism deficiency | (Orphanet:217566) |
| Combined pulmonary fibrosis-emphysema syndrome | (Orphanet:300564) |
| DK1-CDG | (Orphanet:91131) |
| Desquamative interstitial pneumonia | (Orphanet:98852) |
| Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease | (Orphanet:439854) |
| Gaucher disease type 1 | (Orphanet:77259) |
| Gaucher disease type 2 | (Orphanet:77260) |
| Gaucher disease type 3 | (Orphanet:77261) |
| HEMOGLOBIN--ALPHA LOCUS 1 | (OMIM:141800) |
| HEMOGLOBIN--BETA LOCUS | (OMIM:141900) |
| HYPOADRENOCORTICISM, FAMILIAL | (OMIM:240200) |
| Heart tumor of the child | (Orphanet:875) |
| Hemoglobinopathy Toms River | (Orphanet:280615) |
| Hereditary hemorrhagic telangiectasia | (Orphanet:774) |
| His bundle tachycardia | (Orphanet:3283) |
| Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
| Idiopathic pulmonary alveolar proteinosis | (Orphanet:747) |
| Idiopathic pulmonary fibrosis | (Orphanet:2032) |
| Incessant infant ventricular tachycardia | (Orphanet:45453) |
| Laryngo-tracheo-esophageal cleft | (Orphanet:2004) |
| Laryngo-tracheo-esophageal cleft type 3 | (Orphanet:93940) |
| Leprechaunism | (Orphanet:508) |
| Lymphoid interstitial pneumonia | (Orphanet:79128) |
| METHEMOGLOBINEMIA TYPE IV | (OMIM:250790) |
| Mucopolysaccharidosis type 2, severe form | (Orphanet:217085) |
| Naxos disease | (Orphanet:34217) |
| Neonatal acute respiratory distress with surfactant metabolism deficiency | (Orphanet:217563) |
| Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
| Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
| OBESITY-HYPOVENTILATION SYNDROME | (OMIM:257500) |
| Phosphoenolpyruvate carboxykinase 1 deficiency | (Orphanet:79316) |
| Pulmonary arteriovenous fistula | (Orphanet:2038) |
| Pulmonary capillary hemangiomatosis | (Orphanet:199241) |
| Pulmonary venoocclusive disease | (Orphanet:31837) |
| Recessive hereditary methemoglobinemia type 1 | (Orphanet:139373) |
| Recessive hereditary methemoglobinemia type 2 | (Orphanet:139380) |
| Reticular dysgenesis | (Orphanet:33355) |
| SEIZURES, BENIGN FAMILIAL INFANTILE, 1 | (OMIM:601764) |
| SULFHEMOGLOBINEMIA, CONGENITAL | (OMIM:185460) |
| SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1 | (OMIM:265120) |
| TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER | (OMIM:187300) |
| TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 | (OMIM:600376) |
| TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4 | (OMIM:610655) |
| Tropical endomyocardial fibrosis | (Orphanet:75565) |
| VENULAR INSUFFICIENCY, SYSTEMIC | (OMIM:192700) |
| [DEL] GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL | (OMIM:261740) |