Delayed puberty

Symptom Information:

Symptom ID: HPO:0000823
Synonyms:
Delalyed puberty [HPO:0000823]
Delayed pubertal development [HPO:0000823]
Delayed pubertal growth [HPO:0000823]
Delayed puberty (female) [HPO:0000823]
Delayed puberty (male) [HPO:0000823]
Late puberty [Orphanet:41780]
Delalyed puberty [OMIM:Delalyed puberty]
Delayed pubertal development [OMIM:Delayed pubertal development]
Delayed pubertal growth [OMIM:Delayed pubertal growth]
Delayed puberty [OMIM:Delayed puberty]
Late puberty/hypogonadism/hypogenitalism [Orphanet:41780]
Delayed puberty [MedDRA:10012205]
Delayed or incomplete puberty (1 family) [OMIM
du]
Quality:
Cross references:
Orphanet:41780 "Late puberty/hypogonadism/hypogenitalism" [Orphanet:41780]
OMIM: "Delalyed puberty" [OMIM:Delalyed puberty]
OMIM: "Delayed pubertal development" [OMIM:Delayed pubertal development]
OMIM: "Delayed pubertal growth" [OMIM:Delayed pubertal growth]
OMIM: "Delayed puberty" [OMIM:Delayed puberty]
Is a (Direct Parents):
HPO         Growth delay
Orphanet Hypogonadism
Orphanet Abnormality of the endocrine system
HPO         Puberty and gonadal disorders
MedDRA Endocrine abnormalities of puberty
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Growth abnormality(HPO:0001507)
          Growth delay(HPO:0001510)
             Delayed puberty(HPO:0000823)
       Abnormality of the endocrine system(HPO:0000818)
          Puberty and gonadal disorders(HPO:0008373)
             Delayed puberty(HPO:0000823)
MedDRA:
Endocrine disorders(MedDRA:10014698)
    Endocrine disorders of gonadal function(MedDRA:10014701)
       Endocrine abnormalities of puberty(MedDRA:10014692)
          Delayed puberty(HPO:0000823)
Database Frequency: 65 / 7739
Resource:

All diseases associated with this symptom:

46,XY complete gonadal dysgenesis (Orphanet:242)
48,XXYY syndrome (Orphanet:10)
AARSKOG-SCOTT SYNDROME (OMIM:305400)
ACID-LABILE SUBUNIT DEFICIENCY (OMIM:615961)
ADRENAL HYPOPLASIA, CONGENITAL (OMIM:300200)
ANE syndrome (Orphanet:157954)
ARTERIOSCLEROSIS, SEVERE JUVENILE (OMIM:208060)
ATAXIA-TELANGIECTASIA (OMIM:208900)
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET (OMIM:615952)
Absent thumb - short stature - immunodeficiency (Orphanet:2951)
Alström syndrome (Orphanet:64)
Ataxia-telangiectasia (Orphanet:100)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
Bangstad syndrome (Orphanet:1227)
Bardet-Biedl syndrome (Orphanet:110)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Barth syndrome (Orphanet:111)
Borjeson-Forssman-Lehmann syndrome (Orphanet:127)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
CHARGE syndrome (Orphanet:138)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Cabezas syndrome (Orphanet:85293)
Camurati-Engelmann disease (Orphanet:1328)
Cohen syndrome (Orphanet:193)
Costello syndrome (Orphanet:3071)
Cystinosis (Orphanet:213)
Fabry disease (Orphanet:324)
GLYCOGEN STORAGE DISEASE Ic (OMIM:232240)
GOMBO SYNDROME (OMIM:233270)
Gaucher disease type 1 (Orphanet:77259)
Glycogen storage disease due to aldolase A deficiency (Orphanet:57)
Glycogen storage disease due to glucose-6-phosphatase deficiency (Orphanet:364)
Glycogen storage disease due to glucose-6-phosphatase deficiency type a (Orphanet:79258)
Glycogen storage disease due to glucose-6-phosphatase deficiency type b (Orphanet:79259)
HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA (OMIM:614841)
HYPOGONADOTROPIC HYPOGONADISM 20 WITH OR WITHOUT ANOSMIA (OMIM:615270)
Hemochromatosis type 2 (Orphanet:79230)
Hemochromatosis, type 2A (OMIM:602390)
IMMUNODEFICIENCY 31C (OMIM:614162)
Insulin-resistance syndrome type A (Orphanet:2297)
Kostmann syndrome (Orphanet:99749)
LEOPARD SYNDROME 1 (OMIM:151100)
Leukoencephalopathy - ataxia - hypodontia - hypomyelination (Orphanet:137639)
MELAS (Orphanet:550)
MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM (OMIM:616033)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Mitochondrial myopathy and sideroblastic anemia (Orphanet:2598)
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism (Orphanet:280679)
Myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1 (OMIM:600462)
Noonan syndrome (Orphanet:648)
Noonan syndrome with multiple lentigines (Orphanet:500)
Obesity due to leptin receptor gene deficiency (Orphanet:179494)
POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY,AND PULMONARY FIBROSIS (OMIM:615704)
Prader-Willi syndrome (Orphanet:739)
Progeria - short stature - pigmented nevi (Orphanet:2959)
Roifman syndrome (Orphanet:353298)
Ruvalcaba syndrome (Orphanet:3121)
Spastic paraplegia 64, autosomal recessive (OMIM:615683)
Trichomegaly - retina pigmentary degeneration - dwarfism (Orphanet:3363)
Ulnar-mammary syndrome (Orphanet:3138)
Werner syndrome (Orphanet:902)
Wilson-Turner syndrome (Orphanet:3459)
Wolfram syndrome (Orphanet:3463)
Woodhouse-Sakati syndrome (Orphanet:3464)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)