Growth hormone deficiency
Symptom Information:
Symptom ID: | HPO:0000824 | |||||||
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) Abnormality of the endocrine system(HPO:0000818) Abnormality of the hypothalamus-pituitary axis(HPO:0000864) Abnormality of the pituitary gland(HPO:0012503) Abnormality of the anterior pituitary(HPO:0011747) Anterior hypopituitarism(HPO:0000830) Growth hormone deficiency(HPO:0000824) Abnormality of circulating hormone level(HPO:0003117) Growth hormone deficiency(HPO:0000824) MedDRA: Endocrine disorders(MedDRA:10014698) Hypothalamus and pituitary gland disorders(MedDRA:10021112) Anterior pituitary hypofunction(MedDRA:10002701) Growth hormone deficiency(HPO:0000824) |
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Database Frequency: | 56 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
15q24 microdeletion syndrome | (Orphanet:94065) |
2p21 microdeletion syndrome | (Orphanet:163693) |
3C syndrome | (Orphanet:7) |
ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM,AND TRACHEAL STENOSIS | (OMIM:601427) |
ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION,AND FACIAL ANOMALIES | (OMIM:208080) |
AXENFELD-RIEGER SYNDROME, TYPE 1 | (OMIM:180500) |
Acro-oto-ocular syndrome | (Orphanet:2980) |
Alström syndrome | (Orphanet:64) |
Atypical hypotonia - cystinuria syndrome | (Orphanet:238523) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
Axenfeld-Rieger syndrome | (Orphanet:782) |
Bonnemann-Meinecke-Reich syndrome | (Orphanet:1261) |
CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURALHEARING LOSS, AND SKELETAL DYSPLASIA | (OMIM:616007) |
CHARGE syndrome | (Orphanet:138) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Cohen syndrome | (Orphanet:193) |
Combined oxidative phosphorylation defect type 15 | (Orphanet:319524) |
Costello syndrome | (Orphanet:3071) |
Dent disease type 1 | (Orphanet:93622) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 | (OMIM:129900) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 | (OMIM:604292) |
EEC syndrome | (Orphanet:1896) |
Faisalabad histiocytosis | (Orphanet:254707) |
Gómez-López-Hernández syndrome | (Orphanet:1532) |
H syndrome | (Orphanet:168569) |
HOLOPROSENCEPHALY 9 | (OMIM:610829) |
Hypotonia - cystinuria syndrome | (Orphanet:163690) |
IMAGe syndrome | (Orphanet:85173) |
IMMUNODEFICIENCY, COMMON VARIABLE, 10 | (OMIM:615577) |
Isolated growth hormone deficiency type IB | (Orphanet:231671) |
Isolated growth hormone deficiency type II | (Orphanet:231679) |
Isolated growth hormone deficiency type III | (Orphanet:231692) |
Juberg-Hayward syndrome | (Orphanet:2319) |
Laron syndrome with immunodeficiency | (Orphanet:220465) |
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2 | (OMIM:614114) |
MOVED TO 614732 | (OMIM:300290) |
Monosomy 18q | (Orphanet:1600) |
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism | (Orphanet:280679) |
Nonacquired combined pituitary hormone deficiency with spine abnormalities | (Orphanet:231720) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Obesity due to leptin receptor gene deficiency | (Orphanet:179494) |
PITUITARY DWARFISM WITH LARGE SELLA TURCICA | (OMIM:262710) |
Pallister-Hall syndrome | (Orphanet:672) |
Pigmented hypertrichosis with insulin dependent diabetes mellitus syndrome | (Orphanet:254723) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Prader-Willi syndrome | (Orphanet:739) |
RHYNS syndrome | (Orphanet:140976) |
Rosaï-Dorfman disease | (Orphanet:158014) |
Septo-optic dysplasia | (Orphanet:3157) |
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia | (Orphanet:632) |
Silver-Russell syndrome | (Orphanet:813) |
Solitary median maxillary central incisor syndrome | (Orphanet:2286) |
Trichomegaly - retina pigmentary degeneration - dwarfism | (Orphanet:3363) |
WEBB-DATTANI SYNDROME | (OMIM:615926) |
Wolfram syndrome 1 | (OMIM:222300) |