Abnormality of the vagina
Symptom Information:
Symptom ID: | HPO:0000142 | |||||||||||||||||
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 genitourinary system(HPO:0000119) Abnormality of the genital system(HPO:0000078) Abnormal genital system morphology(HPO:0012243) Abnormal internal genitalia(HPO:0000812) Abnormality of female internal genitalia(HPO:0000008) Abnormality of the vagina(HPO:0000142) Abnormality of the female genitalia(HPO:0010460) Abnormality of female internal genitalia(HPO:0000008) Abnormality of the vagina(HPO:0000142) MedDRA: |
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Database Frequency: | 24 / 7739 | |||||||||||||||||
Resource: |
All diseases associated with this symptom:
AREDYLD syndrome | (Orphanet:1133) |
Adiposis dolorosa | (Orphanet:36397) |
Chronic mucocutaneous candidiasis | (Orphanet:1334) |
Diffuse cutaneous systemic sclerosis | (Orphanet:220393) |
Double uterus - hemivagina - renal agenesis | (Orphanet:3411) |
Fraser syndrome | (Orphanet:2052) |
HYDROLETHALUS SYNDROME 1 | (OMIM:236680) |
HYMEN, IMPERFORATE | (OMIM:237100) |
Hydrolethalus | (Orphanet:2189) |
Kallmann syndrome | (Orphanet:478) |
Langer-Giedion syndrome | (Orphanet:502) |
Lyell syndrome | (Orphanet:537) |
McKusick-Kaufman syndrome | (Orphanet:2473) |
Meacham syndrome | (Orphanet:3097) |
Peritoneal cystic mesothelioma | (Orphanet:168816) |
Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
Scleroderma | (Orphanet:801) |
Stevens-Johnson syndrome | (Orphanet:36426) |
Systemic sclerosis | (Orphanet:90291) |
Tetraamelia - multiple malformations | (Orphanet:3301) |
Townes-Brocks syndrome | (Orphanet:857) |
Ulnar-mammary syndrome | (Orphanet:3138) |
WAGR syndrome | (Orphanet:893) |
Waardenburg syndrome | (Orphanet:3440) |