Hypoplasia of the uterus

Symptom Information:

Symptom ID: HPO:0000013
Synonyms:
Hypoplastic uterus [HPO:0000013]
Rudimentary uterus [HPO:0000013]
Hypoplastic uterus [OMIM:Hypoplastic uterus]
Rudimentary uterus [OMIM:Rudimentary uterus]
Quality:
Cross references:
OMIM: "Hypoplastic uterus" [OMIM:Hypoplastic uterus]
OMIM: "Rudimentary uterus" [OMIM:Rudimentary uterus]
Is a (Direct Parents):
HPO         Aplasia/hypoplasia of the uterus
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)
                            Hypoplasia of the uterus(HPO:0000013)
                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)
                            Hypoplasia of the uterus(HPO:0000013)
MedDRA:
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

46,XX testicular disorder of sex development (Orphanet:393)
46,XY SEX REVERSAL 7 (OMIM:233420)
46,XY complete gonadal dysgenesis (Orphanet:242)
Autosomal dominant popliteal pterygium syndrome (Orphanet:1300)
CHONDRODYSPLASIA, ACROMESOMELIC, WITH GENITAL ANOMALIES (OMIM:609441)
Classic Mayer-Rokitansky-Küster-Hauser syndrome (Orphanet:247775)
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency (Orphanet:90795)
HYPOGONADOTROPIC HYPOGONADISM 13 WITH OR WITHOUT ANOSMIA (OMIM:614842)
HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA (OMIM:614837)
Insulin-resistance syndrome type A (Orphanet:2297)
MICROPHTHALMIA, SYNDROMIC 7 (OMIM:309801)
MURCS association (Orphanet:2578)
Matthew-Wood syndrome (Orphanet:2470)
Mulibrey nanism (Orphanet:2576)
Perrault Syndrome 1 (OMIM:233400)
Perrault Syndrome 3 (OMIM:614129)
Perrault Syndrome 4 (OMIM:615300)
Peters-plus syndrome (Orphanet:709)
Renal cysts and diabetes syndrome (Orphanet:93111)
SATOYOSHI SYNDROME (OMIM:600705)
Woodhouse-Sakati syndrome (Orphanet:3464)