Delayed menarche

Symptom Information:

Symptom ID: HPO:0012569
Synonyms:
Delayed menarche. [OMIM:Delayed menarche.]
Delayed menarche [MedDRA:10063961]
Quality:
Cross references:
OMIM: "Delayed menarche." [OMIM:Delayed menarche.]
Is a (Direct Parents):
HPO         Abnormality of the menstrual cycle
HPO         Delayed puberty
MedDRA Menstruation and uterine bleeding NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Growth abnormality(HPO:0001507)
          Growth delay(HPO:0001510)
             Delayed puberty(HPO:0000823)
                Delayed menarche(HPO:0012569)
       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 menstrual cycle(HPO:0000140)
                         Delayed menarche(HPO:0012569)
                Abnormal internal genitalia(HPO:0000812)
                   Abnormality of female internal genitalia(HPO:0000008)
                      Abnormality of the menstrual cycle(HPO:0000140)
                         Delayed menarche(HPO:0012569)
       Abnormality of the endocrine system(HPO:0000818)
          Puberty and gonadal disorders(HPO:0008373)
             Delayed puberty(HPO:0000823)
                Delayed menarche(HPO:0012569)
             Abnormality of the menstrual cycle(HPO:0000140)
                Delayed menarche(HPO:0012569)
MedDRA:
Reproductive system and breast disorders(MedDRA:10038604)
    Menstrual cycle and uterine bleeding disorders(MedDRA:10013326)
       Menstruation and uterine bleeding NEC(MedDRA:10027335)
          Delayed menarche(HPO:0012569)
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Hemochromatosis, type 2A (OMIM:602390)
Hurler-Scheie syndrome (Orphanet:93476)
Laron syndrome (Orphanet:633)
Noonan syndrome with multiple lentigines (Orphanet:500)
Wolfram syndrome 2 (OMIM:604928)