Hydrocele testis
Symptom Information:
Symptom ID: | HPO:0000034 | |||||||||||||||||||
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 genitourinary system(HPO:0000119) Abnormality of the genital system(HPO:0000078) Abnormal genital system morphology(HPO:0012243) Abnormal internal genitalia(HPO:0000812) Abnormality of male internal genitalia(HPO:0000022) Abnormality of the testis(HPO:0000035) Hydrocele testis(HPO:0000034) Abnormality of the male genitalia(HPO:0010461) Abnormality of male internal genitalia(HPO:0000022) Abnormality of the testis(HPO:0000035) Hydrocele testis(HPO:0000034) MedDRA: Reproductive system and breast disorders(MedDRA:10038604) Penile and scrotal disorders (excl infections and inflammations)(MedDRA:10013355) Scrotal disorders NEC(MedDRA:10039745) Hydrocele testis(HPO:0000034) |
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Database Frequency: | 18 / 7739 | |||||||||||||||||||
Resource: |
All diseases associated with this symptom:
COWDEN SYNDROME 5 | (OMIM:615108) |
COWDEN SYNDROME 6 | (OMIM:615109) |
Cowden syndrome | (Orphanet:201) |
Glomerulonephritis - sparse hair - telangiectasis | (Orphanet:2087) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hypotrichosis - lymphedema - telangiectasia | (Orphanet:69735) |
LYMPHEDEMA, HEREDITARY, IA | (OMIM:153100) |
LYMPHEDEMA, HEREDITARY, ID | (OMIM:615907) |
Leprechaunism | (Orphanet:508) |
Lhermitte-Duclos disease | (Orphanet:65285) |
Lymphedema - atrial septal defects - facial changes | (Orphanet:86915) |
Milroy disease | (Orphanet:79452) |
Multiple congenital anomalies - hypotonia - seizures syndrome | (Orphanet:280633) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Proteus-like syndrome | (Orphanet:2969) |
RENAL AND MULLERIAN DUCT HYPOPLASIA | (OMIM:266810) |
Weaver syndrome | (Orphanet:3447) |