Delayed puberty
Symptom Information:
Symptom ID: | HPO:0000823 | ||||||||||||||
Synonyms: |
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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) 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) |
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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) |