Pallor
Symptom Information:
Symptom ID: | HPO:0000980 | |||||||||||||||||||||||
Synonyms: |
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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) Abnormality of skin morphology(HPO:0011121) Pallor(HPO:0000980) MedDRA: Vascular disorders(MedDRA:10047065) Vascular disorders NEC(MedDRA:10047066) Site specific vascular disorders NEC(MedDRA:10057188) Pallor(HPO:0000980) |
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Database Frequency: | 52 / 7739 | |||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib | (OMIM:615631) |
Alport syndrome | (Orphanet:63) |
Autoimmune hemolytic anemia | (Orphanet:98375) |
Autoimmune hemolytic anemia, cold type | (Orphanet:228312) |
Autoimmune hemolytic anemia, warm type | (Orphanet:90033) |
Autosomal recessive malignant osteopetrosis | (Orphanet:667) |
BREATH-HOLDING SPELLS | (OMIM:607578) |
Beta-thalassemia | (Orphanet:848) |
Beta-thalassemia major | (Orphanet:231214) |
Blackfan-Diamond anemia | (Orphanet:124) |
CREST syndrome | (Orphanet:90290) |
CYCLIC VOMITING SYNDROME | (OMIM:500007) |
Choreoacanthocytosis | (Orphanet:2388) |
Cold agglutinin disease | (Orphanet:56425) |
Combined oxidative phosphorylation defect type 4 | (Orphanet:254925) |
Constitutional megaloblastic anemia with severe neurologic disease | (Orphanet:319651) |
Criss-cross heart | (Orphanet:1461) |
DERMATITIS, ATOPIC | (OMIM:603165) |
DIAMOND-BLACKFAN ANEMIA 1 | (OMIM:105650) |
Deafness - lymphedema - leukemia | (Orphanet:3226) |
Dehydrated hereditary stomatocytosis | (Orphanet:3202) |
Dominant beta-thalassemia | (Orphanet:231226) |
Drug-induced autoimmune hemolytic anemia | (Orphanet:90037) |
Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency | (Orphanet:289527) |
Fumaric aciduria | (Orphanet:24) |
Gaucher disease - ophthalmoplegia - cardiovascular calcification | (Orphanet:2072) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type a | (Orphanet:79258) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
Hb Bart's hydrops fetalis | (Orphanet:163596) |
Hereditary folate malabsorption | (Orphanet:90045) |
Hereditary persistence of fetal hemoglobin - beta-thalassemia | (Orphanet:46532) |
Hurler syndrome | (Orphanet:93473) |
Leber congenital amaurosis 14 | (OMIM:613341) |
Leprechaunism | (Orphanet:508) |
Letterer-Siwe disease | (Orphanet:99870) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 3 | (OMIM:253280) |
Methylmalonic acidemia with homocystinuria, type cblC | (Orphanet:79282) |
Methylmalonic acidemia with homocystinuria, type cblD | (Orphanet:79283) |
Mixed-type autoimmune hemolytic anemia | (Orphanet:90036) |
Monosomy 9p | (Orphanet:261112) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
Myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1 | (OMIM:600462) |
Pearson syndrome | (Orphanet:699) |
RETINITIS PIGMENTOSA 42 | (OMIM:612943) |
Retinohepatoendocrinologic syndrome | (Orphanet:3087) |
Rheumatic fever | (Orphanet:3099) |
Spontaneous periodic hypothermia | (Orphanet:29822) |
Waldenström macroglobulinemia | (Orphanet:33226) |
Wilson disease | (Orphanet:905) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |