Growth hormone deficiency

Symptom Information:

Symptom ID: HPO:0000824
Synonyms:
Growth hormone deficiency [OMIM:Growth hormone deficiency]
Growth hormone deficiency (2 patients) [OMIM:Growth hormone deficiency (2 patients)]
Growth hormone deficiency (HCS) [OMIM:Growth hormone deficiency (HCS)]
Growth hormone deficiency (in 1/4 patients) [OMIM:Growth hormone deficiency (in 1/4 patients)]
Growth hormone deficiency (rare) [OMIM:Growth hormone deficiency (rare)]
Growth hormone deficiency (reported in 1 patient) [OMIM:Growth hormone deficiency (reported in 1 patient)]
Growth hormone deficiency [MedDRA:10056438]
Quality:
Cross references:
OMIM: "Growth hormone deficiency" [OMIM:Growth hormone deficiency]
OMIM: "Growth hormone deficiency (2 patients)" [OMIM:Growth hormone deficiency (2 patients)]
OMIM: "Growth hormone deficiency (HCS)" [OMIM:Growth hormone deficiency (HCS)]
OMIM: "Growth hormone deficiency (in 1/4 patients)" [OMIM:Growth hormone deficiency (in 1/4 patients)]
OMIM: "Growth hormone deficiency (rare)" [OMIM:Growth hormone deficiency (rare)]
OMIM: "Growth hormone deficiency (reported in 1 patient)" [OMIM:Growth hormone deficiency (reported in 1 patient)]
Is a (Direct Parents):
HPO         Anterior hypopituitarism
MedDRA Anterior pituitary hypofunction
HPO         Abnormality of circulating hormone level
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)
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)