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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
46,XY complete gonadal dysgenesis +  
adenovirus renal infection 
Adult familial nephronophthisis - spastic quadriparesia 
Aicardi syndrome 
amelogenesis imperfecta type 1G 
aniridia +  
anorectal malformation +   
anterior segment dysgenesis +  
anuria 
Aortic Coarctation +  
aortic valve stenosis +   
atheroembolism of kidney 
atresia of small intestine 
atypical Werner syndrome 
Autosomal dominant medullary cystic kidney disease with hyperuricemia 
autosomal dominant progressive nephropathy with hypertension 
autosomal recessive frontotemporal pachygyria 
axial mesodermal dysplasia spectrum 
Behcet's syndrome  
Berardinelli-Seip congenital lipodystrophy +  
bicornuate uterus 
blepharoptosis-cleft palate-ectrodactyly-dental anomalies syndrome 
Bloom syndrome 
bone development disease +   
brachydactyly +  
branchial arch disease +   
bronchogenic cyst 
bronchopulmonary dysplasia  
camptodactyly of fingers 
cardiac valvular defect, developmental 
cataract - congenital heart disease - neural tube defect syndrome 
cephalocele +  
cerebral cortical dysplasia +  
Cerebro-reno-digital syndrome 
chronic kidney disease +   
Chudley-McCullough syndrome 
CK syndrome 
cleft lip and alveolus +  
cleft lip/palate +  
cleft palate-stapes fixation-oligodontia syndrome 
colonic atresia 
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 patella dislocation +  
congenital primary megaureter +  
congenital short bowel syndrome +  
congenital shoulder dislocation 
congenital tricuspid malformation +  
corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome 
craniodiaphyseal dysplasia 
craniofacial dysplasia - osteopenia syndrome 
craniofacial dyssynostosis 
craniorachischisis 
cystic kidney disease +   
deafness-oligodontia syndrome 
demyelinating disease +   
dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome 
developmental defect during embryogenesis +   
diabetes insipidus +  
diencephalic-mesencephalic junction dysplasia 
distal symphalangism 
DNA ligase IV deficiency 
double uterus-hemivagina-renal agenesis syndrome 
duodenal atresia 
duplication of the pituitary gland 
duplication of urethra 
epibulbar lipodermoid-preauricular appendage-polythelia syndrome 
exstrophy-epispadias complex +   
familial bicuspid aortic valve 
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 
fetal lower urinary tract obstruction +   
Fowler syndrome 
gingival fibromatosis-progressive deafness syndrome 
glomerular disease +   
hantavirus hemorrhagic fever with renal syndrome +  
hemoglobinuria +  
hemorrhagic fever with renal syndrome  
Hepatic fibrosis - renal cysts - intellectual disability 
hereditary cardiac anomaly +  
hereditary gingival fibromatosis 
hereditary lethal multiple congenital anomalies/dysmorphic syndrome +  
high anorectal malformation 
horizontal gaze palsy with progressive scoliosis 
hydronephrosis +   
hypertensive nephropathy +   
hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome 
hypohidrotic ectodermal dysplasia +  
hypospadias  
impaired renal function disease +   
imperforate anus 
Infantile nephronophthisis 
inherited kidney disorder +   
intermediate anorectal malformation 
isolated cerebellar hypoplasia/agenesis 
isolated cleft lip +  
isolated congenital digital clubbing 
Jalili syndrome 
Joubert syndrome +  
Juvenile nephronophthisis 
keratinization disease +   
kidney cortex necrosis 
kidney failure +   
kidney neoplasm +   
kidney papillary necrosis +  
L1 syndrome +  
lissencephaly spectrum disorders +  
loose anagen 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 +  
medullary sponge kidney 
megalencephaly +  
megalodactyly 
microcephaly +  
microcephaly-polymicrogyria-corpus callosum agenesis syndrome 
Morgagni-Stewart-Morel syndrome 
mulibrey nanism 
multicystic dysplastic kidney +  
multiple intestinal atresia 
Nance-Horan syndrome 
natal teeth-intestinal pseudoobstruction-patent ductus syndrome 
nephritis +   
nephrocalcinosis +  
nephrolithiasis +   
nephrosis +   
neurocristopathy +   
non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome 
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 +  
pancreatic agenesis +  
penoscrotal transposition 
pericardial and diaphragmatic defect 
perinephritis 
polydactyly +  
polymyositis +   
porencephaly-microcephaly-bilateral congenital cataract syndrome 
post-operative acute kidney injury  
postaxial polydactyly-dental and vertebral anomalies syndrome 
precocious puberty +   
primary basilar invagination 
progeroid features-hepatocellular carcinoma predisposition syndrome 
progressive cerebello-cerebral atrophy 
progressive microcephaly-seizures-cortical blindness-developmental delay syndrome 
renal agenesis +   
renal aminoaciduria 
renal artery disease +  
renal dysplasia +  
renal glycosuria 
renal hypertension +  
renal hypoplasia +  
Renal hypoplasia is a developmental anomaly in which one or both kidneys (unilateral or bilateral renal hypoplasia, respectively) have a deficit in the number of nephrons and may be small. Oligomeganephronia represents a severe variant of hypoplasia in which nephron number is reduced by 80% and nephrons are markedly hypertrophied.
renal nutcracker syndrome 
renal tuberculosis +  
renal tubular dysgenesis +  
renal tubular dysgenesis of genetic origin 
renal tubular transport disease +  
renal tubule disease +  
Rothmund-Thomson syndrome +  
spina bifida +  
steatocystoma multiplex-natal teeth syndrome 
steroid dehydrogenase deficiency-dental anomalies syndrome 
stricture or kinking of ureter  
syndactyly +  
systemic lupus erythematosus +   
systemic scleroderma +   
T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency 
Takayasu arteritis  
temporal arteritis  
thumb deformity-alopecia-pigmentation anomaly syndrome 
torticollis-keloids-cryptorchidism-renal dysplasia syndrome 
upper limb hypertrophy 
ureteral disorder +   
uterine hypoplasia 
X-linked diffuse leiomyomatosis-Alport syndrome 
X-linked intellectual disability-corpus callosum agenesis-spastic quadriparesis syndrome 

Synonyms
Exact Synonyms: DOID:0080204 ;   Orphanet:93101 ;   http://identifiers.org/medgen/120571 ;   http://identifiers.org/snomedct/32659003 ;   http://linkedlifedata.com/resource/umls/id/C0266295 ;   renal hypoplasia (disease)
Synonyms: http://identifiers.org/meddra/10049102
Alternate IDs: MONDO:0019637
Xrefs: DOID:0080204 ;   GARD:19172 ;   HP:0000089 ;   MEDGEN:120571 ;   MedDRA:10049102 ;   NANDO:2200155 ;   ORDO:93101 ;   SCTID:32659003 ;   UMLS:C0266295
Definition Sources: Orphanet:93101

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