Breast hypoplasia

Symptom Information:

Symptom ID: HPO:0003187
Synonyms:
Underdeveloped breasts [HPO:0003187]
Mammary gland aplasia [Orphanet:15440]
Congenital absence of breast (disorder) [Orphanet:15440]
Absence of breast (finding) [Orphanet:15440]
Congenital absence of breast [Orphanet:15440]
Breast hypoplasia [OMIM:Breast hypoplasia]
Underdeveloped breasts [OMIM:Underdeveloped breasts]
Breast tissue/mammary gland absence/aplasia [Orphanet:15440]
Breast absent [Orphanet:15440]
Amastia [MedDRA:10072717]
Breast absent [MedDRA:10072717]
Amastia [OMIM:Amastia]
Breasts underdeveloped [OMIM:Breasts underdeveloped]
Underdeveloped breasts (rare) [OMIM:Underdeveloped breasts (rare)]
Breast hypoplasia [MedDRA:10049070]
Quality:
Cross references:
HPO:0100783 "Breast aplasia" [Orphanet:15440]
Orphanet:15440 "Breast tissue/mammary gland absence/aplasia" [Orphanet:15440]
OMIM: "Breast hypoplasia" [OMIM:Breast hypoplasia]
OMIM: "Underdeveloped breasts" [OMIM:Underdeveloped breasts]
OMIM: "Amastia" [OMIM:Amastia]
OMIM: "Breasts underdeveloped" [OMIM:Breasts underdeveloped]
OMIM: "Underdeveloped breasts (rare)" [OMIM:Underdeveloped breasts (rare)]
UMLS:C0266009 "Congenital absence of breast" [Orphanet:15440]
UMLS:C0425775 "Absence of breast (finding)" [Orphanet:15440]
Is a (Direct Parents):
Orphanet Abnormality of the thorax
HPO         Aplasia/Hypoplasia of the breasts
MedDRA Breast disorders NEC
HPO         Bilateral breast hypoplasia
HPO         Unilateral breast hypoplasia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the breast(HPO:0000769)
          Aplasia/Hypoplasia of the breasts(HPO:0010311)
             Breast hypoplasia(HPO:0003187)
MedDRA:
Reproductive system and breast disorders(MedDRA:10038604)
    Breast disorders(MedDRA:10006232)
       Breast disorders NEC(MedDRA:10040675)
          Breast hypoplasia(HPO:0003187)
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

46,XY complete gonadal dysgenesis (Orphanet:242)
ADULT syndrome (Orphanet:978)
AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM (OMIM:104350)
AREDYLD syndrome (Orphanet:1133)
ECTODERMAL DYSPLASIA WITH ADRENAL CYST (OMIM:129550)
Ear-patella-short stature syndrome (Orphanet:2554)
Ectodermal dysplasia, tricho-odonto-onychial type (Orphanet:1818)
Fine-Lubinsky syndrome (Orphanet:1272)
GAPO syndrome (Orphanet:2067)
Incontinentia pigmenti (Orphanet:464)
MEIER-GORLIN SYNDROME 1 (OMIM:224690)
MEIER-GORLIN SYNDROME 2 (OMIM:613800)
MEIER-GORLIN SYNDROME 3 (OMIM:613803)
MEIER-GORLIN SYNDROME 4 (OMIM:613804)
OVARIAN DYSGENESIS 3 (OMIM:614324)
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome (Orphanet:314394)
Ulnar-mammary syndrome (Orphanet:3138)