Abnormality of the spleen

Symptom Information:

Symptom ID: HPO:0001743
Synonyms:
Spleen anomaly [Orphanet:31000]
Congenital anomaly of spleen (disorder) [Orphanet:31000]
Congenital anomaly of spleen [Orphanet:31000]
Structural and functional anomalies of the spleen [Orphanet:31000]
Spleen malformation [Orphanet:31000]
Spleen malformation [MedDRA:10062350]
Anomalies of spleen, congenital [MedDRA:10062350]
Congenital anomalies of spleen [MedDRA:10062350]
Congenital spleen anomaly NOS [MedDRA:10062350]
Quality:
Cross references:
Orphanet:31000 "Structural and functional anomalies of the spleen" [Orphanet:31000]
UMLS:C0700587 "Congenital anomaly of spleen" [Orphanet:31000]
Is a (Direct Parents):
HPO         Abnormality of the abdominal organs
HPO         Splenic cyst
MedDRA Spleen disorders
HPO         Abnormality of the lymphatic system
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)
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)