Phimosis
Symptom Information:
Symptom ID: | HPO:0001741 | ||||||||||||
Synonyms: |
|
||||||||||||
Quality: | |||||||||||||
Cross references: |
|
||||||||||||
Is a (Direct Parents): |
|
||||||||||||
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 external genitalia(HPO:0000811) Abnormality of male external genitalia(HPO:0000032) Abnormality of the penis(HPO:0000036) Abnormality of the preputium(HPO:0100587) Phimosis(HPO:0001741) Abnormality of the male genitalia(HPO:0010461) Abnormality of male external genitalia(HPO:0000032) Abnormality of the penis(HPO:0000036) Abnormality of the preputium(HPO:0100587) Phimosis(HPO:0001741) MedDRA: Reproductive system and breast disorders(MedDRA:10038604) Penile and scrotal disorders (excl infections and inflammations)(MedDRA:10013355) Penile disorders NEC (excl erection and ejaculation)(MedDRA:10034304) Phimosis(HPO:0001741) |
||||||||||||
Database Frequency: | 5 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
HEMANGIOMATOSIS, CUTANEOUS, WITH ASSOCIATED FEATURES | (OMIM:234800) |
Hereditary acrokeratotic poikiloderma of Kindler-Weary | (Orphanet:306539) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Lethal acantholytic epidermolysis bullosa | (Orphanet:158687) |
Renpenning syndrome | (Orphanet:3242) |