Pallor

Symptom Information:

Symptom ID: HPO:0000980
Synonyms:
Paleness [HPO:0000980]
Body pale (finding) [Orphanet:54420]
Pale complexion (finding) [Orphanet:54420]
Pallor [Orphanet:54420]
Patient observed to be pale [Orphanet:54420]
Pallor of skin [Orphanet:54420]
Pallor [OMIM:Pallor]
Pale [Orphanet:54420]
Pallor [MedDRA:10033546]
Blanching of skin [MedDRA:10033546]
Complexion ill [MedDRA:10033546]
Looked pale [MedDRA:10033546]
Pale [MedDRA:10033546]
Pale skin [MedDRA:10033546]
Pallor facial [MedDRA:10033546]
Pallor generalized [MedDRA:10033546]
Pallor of skin [MedDRA:10033546]
Pale lips [MedDRA:10033546]
Pale nail beds [MedDRA:10033546]
Blanching [MedDRA:10033546]
Facial pallor [OMIM:Facial pallor]
Pale skin [OMIM:Pale skin]
Pallor (in some patients) [OMIM:Pallor (in some patients)]
Quality:
Cross references:
Orphanet:54420 "Pallor" [Orphanet:54420]
OMIM: "Pallor" [OMIM:Pallor]
OMIM: "Facial pallor" [OMIM:Facial pallor]
OMIM: "Pale skin" [OMIM:Pale skin]
OMIM: "Pallor (in some patients)" [OMIM:Pallor (in some patients)]
UMLS:C0030232 "Pallor" [HPO:0000980]
UMLS:C0030232 "Pallor" [Orphanet:54420]
UMLS:C0678215 "Patient observed to be pale" [Orphanet:54420]
UMLS:C0241137 "Pallor of skin" [Orphanet:54420]
Is a (Direct Parents):
HPO         Abnormality of skin morphology
Orphanet Health status anomalies
MedDRA Site specific vascular disorders NEC
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)
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)