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Hydrophthalmos
Congenital open-angle glaucoma that results from dysgenesis of the angle structures accompanied by increased intraocular pressure and enlargement of the eye. Treatment is both medical and surgical.
推出的年份:
副标题
blood
cerebrospinal fluid
chemically induced
classification
complications
diagnosis
diagnostic imaging
diet therapy
drug therapy
economics
embryology
enzymology
epidemiology
ethnology
etiology
genetics
history
immunology
metabolism
microbiology
mortality
nursing
parasitology
pathology
physiopathology
prevention and control
psychology
radiotherapy
rehabilitation
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therapy
urine
veterinary
virology
树号:
C11.250.480, C11.525.381.407.480, C16.131.384.480, C16.614.438
MeSH 单一 ID:
D006871
进入的组:
Buphthalmos
All MeSH Categories
Diseases Category
Eye Diseases [C11]
Eye Abnormalities [C11.250]
Aniridia [C11.250.060]
add_circle
Anophthalmos [C11.250.080]
Blepharophimosis [C11.250.090]
Choroidal Effusions [C11.250.105]
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Coloboma [C11.250.110]
Ectopia Lentis [C11.250.300]
Familial Exudative Vitreoretinopathies [C11.250.345]
Fraser Syndrome [C11.250.390]
Hydrophthalmos [C11.250.480]
Microphthalmos [C11.250.566]
Persistent Hyperplastic Primary Vitreous [C11.250.616]
Retinal Dysplasia [C11.250.666]
All MeSH Categories
Diseases Category
Eye Diseases [C11]
Ocular Hypertension [C11.525]
Glaucoma [C11.525.381]
Glaucoma, Open-Angle [C11.525.381.407]
Hydrophthalmos [C11.525.381.407.480]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Eye Abnormalities [C16.131.384]
Aniridia [C16.131.384.079]
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Anophthalmos [C16.131.384.159]
Blepharophimosis [C16.131.384.190]
Coloboma [C16.131.384.282]
Ectopia Lentis [C16.131.384.405]
Familial Exudative Vitreoretinopathies [C16.131.384.424]
Fraser Syndrome [C16.131.384.442]
Hydrophthalmos [C16.131.384.480]
Microphthalmos [C16.131.384.666]
Persistent Hyperplastic Primary Vitreous [C16.131.384.725]
Retinal Dysplasia [C16.131.384.784]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Infant, Newborn, Diseases [C16.614]
Amniotic Band Syndrome [C16.614.042]
Anemia, Neonatal [C16.614.053]
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Asphyxia Neonatorum [C16.614.092]
Birth Injuries [C16.614.131]
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Colic [C16.614.166]
Congenital Bone Marrow Failure Syndromes [C16.614.183]
Congenital Hyperinsulinism [C16.614.200]
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Cystic Fibrosis [C16.614.213]
Epilepsy, Benign Neonatal [C16.614.258]
Erythroblastosis, Fetal [C16.614.304]
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Hernia, Umbilical [C16.614.378]
Hydrophthalmos [C16.614.438]
Hyperbilirubinemia, Neonatal [C16.614.451]
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Hyperostosis, Cortical, Congenital [C16.614.465]
Ichthyosis [C16.614.492]
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Infant, Premature, Diseases [C16.614.521]
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Meconium Aspiration Syndrome [C16.614.580]
Mobius Syndrome [C16.614.595]
Neonatal Abstinence Syndrome [C16.614.610]
Neonatal Sepsis [C16.614.627]
Nystagmus, Congenital [C16.614.643]
Ophthalmia Neonatorum [C16.614.677]
Persistent Fetal Circulation Syndrome [C16.614.694]
Rothmund-Thomson Syndrome [C16.614.760]
Sclerema Neonatorum [C16.614.810]
Severe Combined Immunodeficiency [C16.614.815]
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Syphilis, Congenital [C16.614.868]
Thanatophoric Dysplasia [C16.614.890]
Thrombocytopenia, Neonatal Alloimmune [C16.614.899]
Toxoplasmosis, Congenital [C16.614.909]
Vitamin K Deficiency Bleeding [C16.614.940]
Wolman Disease [C16.614.947]
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