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Term:
disorder of development or morphogenesis
(EFO:MONDO:0021147)
Annotations:
Rat: (0)
Mouse: (0)
Human: (2254)
Chinchilla: (0)
Bonobo: (0)
Dog: (0)
Squirrel: (0)
Pig: (0)
Naked Mole-rat: (0)
Green Monkey: (0)
Parent Terms
Term With Siblings
Child Terms
disease
+
acute disease
+
animal disease
+
breast disease
+
cancer or benign tumor
+
cardiovascular disease
+
chromosomal disorder
+
chronic disease
+
complication
+
connective tissue disease
+
digestive system disease
+
disease related to transplantation
+
disorder of development or morphogenesis
+
Any disease or disorder that disrupts the process development of an anatomical structure. Can be due to genetic or environmental causes. Typically happens during embryogenesis, but also includes post-embryonic development.
disorder of visual system
+
endocrine system disease
+
genetic disorder
+
head and neck disorder
+
hematologic disease
+
iatrogenic disease
+
idiopathic disease
+
immune system disease
+
infectious disease
+
inflammatory disease
+
integumentary system disease
+
metabolic disease
+
mitochondrial disease
+
musculoskeletal system disease
+
nervous system disease
+
obstetric disorder
+
occupational disorder
+
otorhinolaryngologic disease
+
perinatal disease
+
perineum disease
poisoning
+
post-infectious disorder
+
premature aging syndrome
+
psychiatric disorder
+
radiation-induced disorder
+
reproductive system disease
+
respiratory system disease
+
soft tissue disease
sudden infant death syndrome
+
syndromic disease
+
ulcer disease
+
upper digestive tract disorder
+
urinary system disease
+
urogenital neoplasm
+
46,XY complete gonadal dysgenesis
+
Aicardi syndrome
amelogenesis imperfecta type 1G
aniridia
+
anorectal malformation
+
anterior segment dysgenesis
+
Aortic Coarctation
+
aortic valve stenosis
+
atresia of small intestine
atypical Werner syndrome
autosomal recessive frontotemporal pachygyria
axial mesodermal dysplasia spectrum
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
+
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
deafness-oligodontia syndrome
demyelinating disease
+
dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome
developmental defect during embryogenesis
+
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
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
Fowler syndrome
gingival fibromatosis-progressive deafness syndrome
hereditary cardiac anomaly
+
hereditary gingival fibromatosis
hereditary lethal multiple congenital anomalies/dysmorphic syndrome
+
high anorectal malformation
horizontal gaze palsy with progressive scoliosis
hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome
hypohidrotic ectodermal dysplasia
+
hypospadias
imperforate anus
intermediate anorectal malformation
isolated cerebellar hypoplasia/agenesis
isolated cleft lip
+
isolated congenital digital clubbing
Jalili syndrome
Joubert syndrome
+
keratinization disease
+
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
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
polydactyly
+
porencephaly-microcephaly-bilateral congenital cataract syndrome
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 dysplasia
+
renal hypoplasia
+
renal tubular dysgenesis of genetic origin
Rothmund-Thomson syndrome
+
spina bifida
+
steatocystoma multiplex-natal teeth syndrome
steroid dehydrogenase deficiency-dental anomalies syndrome
syndactyly
+
T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency
thumb deformity-alopecia-pigmentation anomaly syndrome
torticollis-keloids-cryptorchidism-renal dysplasia syndrome
upper limb hypertrophy
uterine hypoplasia
X-linked intellectual disability-corpus callosum agenesis-spastic quadriparesis syndrome
Synonyms
Exact Synonyms:
http://identifiers.org/medgen/1843482 ; http://linkedlifedata.com/resource/umls/id/C0694457 ; http://purl.bioontology.org/ontology/ICD10CM/Q00-Q99
Alternate IDs:
MONDO:0021147
Xrefs:
ICD10CM:Q00-Q99
; MEDGEN:1843482 ; UMLS:C0694457
External Ontologys:
disease_disrupts EFO:GO:0032502 ; in_taxon EFO:NCBITaxon:9606
Definition Sources:
https://orcid.org/0000-0002-6601-2165