Hypoplastic labia majora
Symptom Information:
Symptom ID: | HPO:0000059 | ||||||||||
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 external genitalia(HPO:0000811) External genital hypoplasia(HPO:0003241) Labial hypoplasia(HPO:0000066) Hypoplastic labia majora(HPO:0000059) Abnormality of female external genitalia(HPO:0000055) Abnormality of the labia(HPO:0000058) Labial hypoplasia(HPO:0000066) Hypoplastic labia majora(HPO:0000059) Abnormality of the female genitalia(HPO:0010460) Abnormality of female external genitalia(HPO:0000055) Abnormality of the labia(HPO:0000058) Labial hypoplasia(HPO:0000066) Hypoplastic labia majora(HPO:0000059) MedDRA: |
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Database Frequency: | 22 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Antley-Bixler syndrome | (Orphanet:83) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal dominant popliteal pterygium syndrome | (Orphanet:1300) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Bartsocas-Papas syndrome | (Orphanet:1234) |
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency | (Orphanet:329255) |
Blepharophimosis-intellectual deficit syndrome, Verloes type | (Orphanet:293725) |
Cornelia de Lange syndrome | (Orphanet:199) |
Distal arthrogryposis type 5D | (Orphanet:329457) |
Ear-patella-short stature syndrome | (Orphanet:2554) |
Femoral-facial syndrome | (Orphanet:1988) |
Gorlin-Chaudhry-Moss syndrome | (Orphanet:2095) |
Kapur-Toriello syndrome | (Orphanet:2328) |
MEIER-GORLIN SYNDROME 1 | (OMIM:224690) |
MEIER-GORLIN SYNDROME 2 | (OMIM:613800) |
Peters-plus syndrome | (Orphanet:709) |
RAPP-HODGKIN SYNDROME | (OMIM:129400) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Schinzel-Giedion syndrome | (Orphanet:798) |
Tetrasomy 12p | (Orphanet:884) |
WARBURG MICRO SYNDROME 2 | (OMIM:614225) |