Abnormality of the spleen
Symptom Information:
Symptom ID: | HPO:0001743 | |||||||||
Synonyms: |
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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 immune system(HPO:0002715) Abnormality of the lymphatic system(HPO:0100763) Abnormality of the spleen(HPO:0001743) Abnormality of the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the spleen(HPO:0001743) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Spleen, lymphatic and reticuloendothelial system disorders(MedDRA:10041641) Spleen disorders(MedDRA:10041635) Abnormality of the spleen(HPO:0001743) |
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Database Frequency: | 37 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
12q14 microdeletion syndrome | (Orphanet:94063) |
1p36 deletion syndrome | (Orphanet:1606) |
Acrocephalosyndactyly | (Orphanet:946) |
Axial mesodermal dysplasia spectrum | (Orphanet:1834) |
CEPHALIN LIPIDOSIS | (OMIM:212800) |
Cantrell pentalogy | (Orphanet:1335) |
Cholestasis - lymphedema | (Orphanet:1414) |
Congenital alveolar capillary dysplasia | (Orphanet:210122) |
Diabetic embryopathy | (Orphanet:1926) |
Feingold syndrome | (Orphanet:1305) |
Fetal Gaucher disease | (Orphanet:85212) |
GM1 gangliosidosis type 2 | (Orphanet:79256) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Holoprosencephaly | (Orphanet:2162) |
Infantile neuronal ceroid lipofuscinosis | (Orphanet:79263) |
Laryngo-tracheo-esophageal cleft - pulmonary hypoplasia | (Orphanet:2005) |
Lower limb deficiency - hypospadias | (Orphanet:2487) |
Matthew-Wood syndrome | (Orphanet:2470) |
Meacham syndrome | (Orphanet:3097) |
Meckel syndrome | (Orphanet:564) |
Microgastria - limb reduction defect | (Orphanet:2538) |
Mosaic trisomy 9 | (Orphanet:99776) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Osteocraniostenosis | (Orphanet:2763) |
PAGOD syndrome | (Orphanet:991) |
Proteus syndrome | (Orphanet:744) |
Reticular dysgenesis | (Orphanet:33355) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Splenogonadal fusion - limb defects - micrognathia | (Orphanet:2063) |
Stormorken-Sjaastad-Langslet syndrome | (Orphanet:3204) |
TUFTSIN DEFICIENCY | (OMIM:191150) |
Tyrosinemia type 1 | (Orphanet:882) |
X-linked sideroblastic anemia | (Orphanet:75563) |