Aplasia of the uterus
Symptom Information:
Symptom ID: | HPO:0000151 | ||
Synonyms: |
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Quality: | |||
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) Abnormality of the female genitalia(HPO:0010460) Abnormality of female internal genitalia(HPO:0000008) Abnormality of the uterus(HPO:0000130) Aplasia/hypoplasia of the uterus(HPO:0008684) Aplasia of the uterus(HPO:0000151) Abnormal internal genitalia(HPO:0000812) Abnormality of female internal genitalia(HPO:0000008) Abnormality of the uterus(HPO:0000130) Aplasia/hypoplasia of the uterus(HPO:0008684) Aplasia of the uterus(HPO:0000151) MedDRA: |
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Database Frequency: | 12 / 7739 | ||
Resource: |
All diseases associated with this symptom:
17q12 microdeletion syndrome | (Orphanet:261265) |
46,XY complete gonadal dysgenesis | (Orphanet:242) |
Atypical Mayer-Rokitansky-Küster-Hauser syndrome | (Orphanet:247768) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
Coffin-Siris syndrome | (Orphanet:1465) |
Phocomelia, Schinzel type | (Orphanet:2879) |
RENAL AND MULLERIAN DUCT HYPOPLASIA | (OMIM:266810) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Spondylocostal dysostosis - anal and genitourinary malformations | (Orphanet:94095) |
Tetrasomy 12p | (Orphanet:884) |
Thrombocytopenia - absent radius | (Orphanet:3320) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |