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Term:
Parent Terms Term With Siblings Child Terms
17,20-lyase deficiency, isolated 
17-alpha-hydroxylase/17,20-lyase deficiency, combined complete 
17-alpha-hydroxylase/17,20-lyase deficiency, combined partial 
46,XY complete gonadal dysgenesis +  
AA amyloidosis 
Adamantinomatous Craniopharyngioma 
Adie syndrome 
adrenal gland disease +   
Aicardi syndrome 
AL amyloidosis +   
Alien Hand Syndrome 
amelogenesis imperfecta type 1G 
aniridia +  
anorectal malformation +   
anterior segment dysgenesis +  
Aortic Coarctation +  
aortic valve stenosis +   
atactic disorder +   
atresia of small intestine 
atypical Werner syndrome 
autoimmune disorder of endocrine system +   
autoimmune disorder of the nervous system +   
autosomal recessive frontotemporal pachygyria 
axial mesodermal dysplasia spectrum 
Bamforth-Lazarus syndrome 
Barre-Lieou syndrome 
Berardinelli-Seip congenital lipodystrophy +  
beta thalassemia +  
bicornuate uterus 
blepharophimosis - intellectual disability syndrome, SBBYS type 
blepharoptosis-cleft palate-ectrodactyly-dental anomalies syndrome 
Bloom syndrome 
bone development disease +   
brachydactyly +  
branchial arch disease +   
bronchogenic cyst 
bronchopulmonary dysplasia  
campomelic dysplasia 
camptodactyly of fingers 
cardiac valvular defect, developmental 
catalepsy 
cataract - congenital heart disease - neural tube defect syndrome 
central nervous system disease +   
central nervous system malformation +  
cephalocele +  
cerebral cortical dysplasia +  
cerebrospinal fluid otorrhea 
choledocholithiasis 
Chudley-McCullough syndrome 
CK syndrome 
cleft lip and alveolus +  
cleft lip/palate +  
cleft palate-stapes fixation-oligodontia syndrome 
colonic atresia 
combined partial 17-alpha-hydroxylase/17,20-lyase deficiency 
complex cortical dysplasia with other brain malformations +  
congenital achiasma 
congenital anomaly of cardiovascular system +   
congenital bilateral absence of vas deferens +  
congenital deformities of limbs +  
congenital elbow dislocation +  
congenital esophageal diverticulum 
congenital hydrocephalus +  
congenital knee dislocation +  
congenital nervous system disorder +  
congenital patella dislocation +  
congenital primary megaureter +  
congenital short bowel syndrome +  
congenital shoulder dislocation 
congenital tricuspid malformation +  
corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome 
cranial nerve neuropathy +   
craniodiaphyseal dysplasia 
craniofacial dysplasia - osteopenia syndrome 
craniofacial dyssynostosis 
craniorachischisis 
Cubital Tunnel Syndrome 
deafness-oligodontia syndrome 
demyelinating disease +   
dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome 
developmental defect during embryogenesis +   
developmental disability +   
diencephalic-mesencephalic junction dysplasia 
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome 
diplegia of upper limb 
disorder of GNAS inactivation +  
disorders of vitamin D metabolism +  
distal symphalangism 
DNA ligase IV deficiency 
dopa-responsive dystonia +  
double uterus-hemivagina-renal agenesis syndrome 
drug-induced akathisia 
drug-Induced dyskinesia  
duodenal atresia 
duplication of the pituitary gland 
duplication of urethra 
endocrine neoplasm +   
endocrine tuberculosis +  
epibulbar lipodermoid-preauricular appendage-polythelia syndrome 
exercise-induced malignant hyperthermia 
familial bicuspid aortic valve 
familial hypocalciuric hypercalcemia +  
familial intestinal malrotation-facial anomalies syndrome 
familial isolated clinodactyly of fingers 
familial isolated congenital asplenia 
familial median cleft of the upper and lower lips 
familial omphalocele syndrome with facial dysmorphism 
familial osteodysplasia, Anderson type 
familial partial lipodystrophy, Dunnigan type 
familial primary pulmonary hypoplasia 
female athlete triad syndrome 
Follicular Variant Thyroid Gland Papillary Carcinoma 
Foster-Kennedy syndrome 
Fowler syndrome 
Genetic endocrine tumor +   
genito-palato-cardiac syndrome 
Gerstmann syndrome 
gingival fibromatosis-progressive deafness syndrome 
gonadal disorder +   
Hand-Arm Vibration Syndrome 
hereditary cardiac anomaly +  
hereditary endocrine growth disease +  
hereditary gingival fibromatosis 
hereditary lethal multiple congenital anomalies/dysmorphic syndrome +  
hereditary neurological disease +   
high anorectal malformation 
horizontal gaze palsy with progressive scoliosis 
hyperinsulinemic hypoglycemia +  
hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome 
hypohidrotic ectodermal dysplasia +  
hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome 
hypoinsulinemic hypoglycemia and body hemihypertrophy 
hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism 
hypospadias  
imperforate anus 
infectious disorder of the nervous system +   
inherited obesity +  
intermediate anorectal malformation 
Isaacs syndrome 
isolated cerebellar hypoplasia/agenesis 
isolated cleft lip +  
isolated congenital digital clubbing 
Jalili syndrome 
Joubert syndrome +  
keratinization disease +   
KIF1A related neurological disorder +  
L1 syndrome +  
Leydig cell hypoplasia +  
Leydig Cell Tumor +  
lissencephaly spectrum disorders +  
liver disease +   
loose anagen syndrome +  
Lopes-Maciel-Rodan syndrome 
low anorectal malformation 
Lowe-Kohn-Cohen syndrome 
lower limb hypertrophy 
lung agenesis-heart defect-thumb anomalies syndrome 
macrocephaly-autism syndrome 
macrodactyly of fingers +  
macrodactyly of toes +  
mbd5 associated neurodevelopmental disorder 
medullary sponge kidney 
megalencephaly +  
megalodactyly 
microcephaly +  
microcephaly-polymicrogyria-corpus callosum agenesis syndrome 
Mixed Somatotroph-Lactotroph Pituitary Gland Adenoma 
Morgagni-Stewart-Morel syndrome 
movement disorder +   
mulibrey nanism 
multicystic dysplastic kidney +  
multiple intestinal atresia 
muscular pseudohypertrophy-hypothyroidism syndrome 
Nance-Horan syndrome 
natal teeth-intestinal pseudoobstruction-patent ductus syndrome 
nervous system heavy metal poisoning +  
nervous system injury +   
nervous system neoplasm +   
neurocristopathy +   
neurocutaneous syndrome +  
Neurodevelopmental disorder +   
neuroendocrine disorder +  
neuroleptic malignant syndrome 
neurological pain disorder +   
neuromuscular disease +   
neuromyelitis optica +   
neuropathy +   
neurosarcoidosis +  
neurovascular disorder +   
NKX2-1 related choreoathetosis and congenital hypothyroidism with or without pulmonary dysfunction +  
non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome 
Non-Neoplastic Bile Duct Disorder +   
Noonan syndrome and Noonan-related syndrome +  
oculocerebral hypopigmentation syndrome, Cross type 
oculodental syndrome, Rutherfurd type 
odontomatosis-aortae esophagus stenosis syndrome 
otodental syndrome 
otofaciocervical syndrome 
overgrowth syndrome +  
pachygyria-intellectual disability-epilepsy syndrome 
pancreas disease +   
pancreatic agenesis +  
Papillary Craniopharyngioma 
Papillary Tumor of the Pineal Region 
paraneoplastic neurologic syndrome +  
parathyroid disease +   
parneoplastic endocrine syndrome +  
penoscrotal transposition 
perceptual disorders +   
pericardial and diaphragmatic defect 
periodic paralysis +   
peripheral nervous system disease +   
phantom limb syndrome 
pituitary deficiency +  
pituitary gland disease +   
polycystic ovary syndrome  
polydactyly +  
polyendocrinopathy +  
Poorly Differentiated Thyroid Gland Carcinoma +  
porencephaly-microcephaly-bilateral congenital cataract syndrome 
postaxial polydactyly-dental and vertebral anomalies syndrome 
Posterior Leukoencephalopathy Syndrome 
precocious puberty +   
primary basilar invagination 
primary orthostatic hypotension +  
progeroid features-hepatocellular carcinoma predisposition syndrome 
progressive cerebello-cerebral atrophy 
progressive microcephaly-seizures-cortical blindness-developmental delay syndrome 
qualitative or quantitative protein defects in neuromuscular diseases +  
radiculitis  
rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome 
Rare genetic endocrine disease +   
renal agenesis +   
renal dysplasia +  
renal hypoplasia +  
renal tubular dysgenesis of genetic origin 
respiratory paralysis 
restless legs syndrome  
retinopathy +   
Rothmund-Thomson syndrome +  
sensory system disease +   
Serotonin Syndrome 
specific language disorder +  
spina bifida +  
spinal cord compression 
steatocystoma multiplex-natal teeth syndrome 
steroid dehydrogenase deficiency-dental anomalies syndrome 
Stiff-Person syndrome 
subacute myelo-opticoneuropathy 
Subdural Effusion 
synaptopathy +  
syndactyly +  
T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency 
thumb deformity-alopecia-pigmentation anomaly syndrome 
thymus gland disorder +  
thymus hyperplasia 
thyroid disease +   
Thyroid Gland Mucosa-Associated Lymphoid Tissue Lymphoma 
Thyroid Gland Oncocytic Follicular Carcinoma 
thyroid hormone metabolism, abnormal +  
torticollis-keloids-cryptorchidism-renal dysplasia syndrome 
toxic encephalopathy +  
tubulinopathy +  
upper limb hypertrophy 
uterine hypoplasia 
wet beriberi 
Wolfram-like syndrome 
Worster-Drought syndrome 
X-linked intellectual disability-corpus callosum agenesis-spastic quadriparesis syndrome 

Synonyms
Exact Synonyms: DPG-plus syndrome ;   Duplication of the pituitary gland-plus syndrome ;   Orphanet:314621 ;   http://identifiers.org/medgen/1663161 ;   http://linkedlifedata.com/resource/umls/id/C4755258 ;   hypophyseal duplication
Alternate IDs: MONDO:0017808
Xrefs: GARD:21381 ;   MEDGEN:1663161 ;   ORDO:314621 ;   UMLS:C4755258

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