Asplenia
Symptom Information:
Symptom ID: | HPO:0001746 | |||||||||||||
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 abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the spleen(HPO:0001743) Aplasia/Hypoplasia of the spleen(HPO:0010451) Asplenia(HPO:0001746) Abnormality of the immune system(HPO:0002715) Abnormality of the lymphatic system(HPO:0100763) Abnormality of the spleen(HPO:0001743) Aplasia/Hypoplasia of the spleen(HPO:0010451) Asplenia(HPO:0001746) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Spleen, lymphatic and reticuloendothelial system disorders(MedDRA:10041641) Spleen disorders(MedDRA:10041635) Asplenia(HPO:0001746) |
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Database Frequency: | 19 / 7739 | |||||||||||||
Resource: |
All diseases associated with this symptom:
Autoimmune polyendocrinopathy type 1 | (Orphanet:3453) |
Autoimmune polyendocrinopathy type 2 | (Orphanet:3143) |
CILIARY DYSKINESIA, PRIMARY, 1 | (OMIM:244400) |
Familial isolated congenital asplenia | (Orphanet:101351) |
Feingold syndrome | (Orphanet:1305) |
HETEROTAXY, VISCERAL, 1, X-LINKED | (OMIM:306955) |
Isolated congenital hypoglossia/aglossia | (Orphanet:141152) |
Ivemark syndrome | (Orphanet:97548) |
LATERALITY DEFECTS, AUTOSOMAL DOMINANT | (OMIM:601086) |
Meckel syndrome | (Orphanet:564) |
Meckel syndrome, type 1 | (OMIM:249000) |
Microgastria - limb reduction defect | (Orphanet:2538) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Osteocraniostenosis | (Orphanet:2763) |
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 | (OMIM:208540) |
RENAL-HEPATIC-PANCREATIC DYSPLASIA 2 | (OMIM:615415) |
Renal-hepatic-pancreatic dysplasia | (Orphanet:294415) |
Stormorken-Sjaastad-Langslet syndrome | (Orphanet:3204) |
Tetraamelia - multiple malformations | (Orphanet:3301) |