mucopolysaccharidosis : Related Words Words similar in meaning to mucopolysaccharidosis
- mucopolysaccharidosis«
- lipochondrodystrophy«
- gargoylism«
- dysostosis multiplex«
- oligosaccharidosis«
- mucopolysaccharidoses«
- mucopolysaccharidotic«
- scheie syndrome«
- inherited disorder«
- metabolic«
- inherited disease«
- lysosomal«
- defective gene«
- hereditary disease«
- glycosaminoglycan«
- hunter syndrome«
- hereditary condition«
- enzyme«
- hurler syndrome«
- genetic disorder«
- disorder«
- child«
- genetic disease«
- sly syndrome«
- genetic defect«
- genetic abnormality«
- sanfilippo syndrome«
- congenital disease«
- enzyme replacement therapy«
- age«
- cornea«
- glycosaminoglycans«
- deficient enzyme«
- mucolipidosis«
- obstructive airway disease«
- heart disease«
- short stature«
- patient«
- neurological complication«
- joint movement«
- nerve root«
- sanfilippo a«
- progressive joint stiffness«
- mp iii disorder«
- cell«
- carpal tunnel syndrome«
- symptom«
- breathing«
- respiratory infection«
- birth«
- skeletal irregularity«
- clouded cornea«
- clinical feature«
- mp disease«
- lamy syndrome«
- hernia«
- maroteaux«
- brain«
- bone«
- mp vi«
- iduronidase«
- fluid«
- lysosomal disease«
- pain«
- mp ii«
- connective tissue«
- ucbt«
- morquio syndrome«
- tissue mass«
- moderate intellectual disability«
- joint stiffness«
- spinal cord«
- adenoid«
- lysosomal storage disease«
- affected child«
- individual«
- inguinal hernia«
- dysplasia«
- organ«
- skeletal structure«
- neurological symptom«
- most child«
- physical symptom«
- parent«
- sleep apnea«
- vision«
- tonsil«
- hydrocephalus«
- developmental delay«
- lysosome«
- hyperactivity«
- loss«
- many child«
- growth«
- aggressive behavior«
- hearing loss«
- glaucoma«
- facial feature«
- person«
- subtypes«
- deafness«
- spleen«
- hurler«
- skin«
- retina«
- missing«
- type b. onset«
- tiny hair cell«
- spinal cervical bone fusion«
- significant corneal«
- sanfilippo d«
- sanfilippo c result«
- sanfilippo b«
- rough facial feature«
- progressive cellular damage«
- pelvic radiography«
- normal reabsorption«
- normal physical strength«
- nighttime oxygen«
- neurosensitive loss«
- mucopolysaccharidosis subtype«
- mp vii«
- mp type«
- mp ix«
- mp iv«
- mp iii«
- mp i. symptom«
- mp i«
- morquios type iv a«
- little clinical difference«
- keratan sulfate sugar chain«
- iduronate sulfatase deficiency«
- hydrocephalus—«
- heparan sulfate sugar chain«
- glucosaminide acetyltransferase«
- enzyme iduronate sulfatase«
- enzymatic replacement therapy«
- endotrachial tube«
- deficient enzyme alpha«
- compressed spinal cord«
- coalpha«
- british columbia estimate«
- bony structure abnormality«
- animal cell malfunction«
- altered enzyme heparan«
- altered enzyme acetyl«
- abnormal bone size«
- traumatized nerve«
- system functioning«
- sugar carbohydrate«
- specialized protein essential«
- shortest survival rate«
- short body trunk«
- shire pharmaceutical group«
- progressive mental decline«
- profound dementia«
- odontoid hypoplasia«
- obstructive airway disorder«
- normal joint movement«
- neurosensory«
- mp type ii«
- mp disorder«
- maximum stature«
- lysosome organelle«
- kenneth d. martin«
- experience periodic bowel«
- excessive cerebrospinal fluid«
- excessive body hair growth«
- excess mucopolysaccharide«
- distinct clinical type«
- australian mp society«
- acetylglucosamine 6-sulfatase«
- unwanted matter«
- systemic irregularity«
- similar compression«
- normal intellectual development«
- lysosomal storage disease family«
- iduronidase deficiency«
- elaprase«
- airway status«
- abnormal physical characteristic«
- body«
- syndrome«
- umbilical cord blood transplantation«
- hand mobility«
- galns«
- diseased heart valve«
- neurologic outcome«
- intracellular storage«
- hyaluronidase deficiency«
- free nerve«
- airway passage«
- acetylgalactosamine 4-sulfatase«
- joint«
- type«
- variable spectrum«
- severe neurological symptom«
- normal intellect«
- nerve root compression«
- lysosomal disorder«
- head—«
- corneal clouding«
- rib«
- nerve«
- incidence«
- unaffected sibling«
- morquio«
- enlarged tongue«
- aldurazyme«
- acetylgalactosamine-6-sulfatase«
- liver«
- severity«
- abdomen«
- surgical insertion«
- excessive mucus«
- enzyme treatment«
- type result«
- irregular sleep«
- clinical subtypes«
- numerous subtypes«
- depressed nasal bridge«
- motor skill development«
- mild learning disability«
- coarse facial feature«
- bone erosion«
- spine«
- simpler molecule«
- noisy breathing«
- impaired motor function«
- biomarin pharmaceutical«
- biomarin«
- stiff joint«
- nerve entrapment«
- fatty material«
- enzyme beta«
- distinct facial feature«
- eye«
- aortic valve disease«
- twenty«
- flat nasal bridge«
- acetylglucosaminidase«
- sulfatase«
- i2s«
- risk procedure«
- diagnosis«
- sugar chain«
- enzyme alpha«
- insufficient level«
- progressive dementia«
- glucuronidase«
- painful swelling«
- most person«
- restricted movement«
- rarest form«
- nerve compression«
- mildest form«
- type a.«
- deformed foot«
- other trait«
- umbilical hernia«
- sugar«
- systemic condition«
- osage city«
- recessive inheritance«
- chest«
- male birth«
- lysosomal enzyme«
- hydrops«
- enzyme assay«
- numerous research project«
- enzyme deficiency«
- marked decline«
- hearing«
- cardiac complication«
- mucopolysaccharide«
- continuous positive airway pressure«
- sleep study«
- malfunctioning«
- survival«
- hip«
- synthetic version«
- unwanted material«
- corneal transplant«
- extensive evaluation«
- skeletal abnormality«
- short trunk«
- intelligence«
- chorionic villus sampling«
- retinal degeneration«
- thick lip«
- galactosidase«
- normal intelligence«
- pelvic region«
- recycling center«
- surgery«
- stage«
- ear drum«
- daily exercise«
- physical growth«
- eventual loss«
- hepatomegaly«
- splenomegaly«
- obstructive sleep apnea«
- extreme amount«
- prenatal diagnosis«
- amniocentesis«
- upper respiratory tract«
- relative«
- average duration«
- nonprofit organisation«
- recessive gene«
- bone marrow transplantation«
- urine test«
- mental function«
- genetic counseling«
- clinical examination«
- physical skill«
- apnea«
- baby«
- spinal nerve«
- autosomal recessive disorder«
- mental development«
- smallness«
- flattening«
- definitive diagnosis«
- disease progression«
- ear infection«
- learning difficulty«
- many individual«
- principal component«
- severe symptom«
- metabolic disorder«
- research network«
- sensory organ«
- middle ear«
- shunt«
- normal development«
- ert«
- respiratory«
- other symptom«
- blood«
- absence«
- cognitive impairment«
- pressure«
- umbilical cord«
- vi.«
- peripheral nervous system«
- damage«
- body fluid«
- united state food«
- teenage«
- type b«
- severe form«
- physical ability«
- dura«
- short neck«
- cerebrospinal fluid«
- night vision«
- dwarfism«
- narrowing«
- excessive amount«
- thickening«
- genetics«
- type a«
- language skill«
- distinct type«
- degeneration«
- height«
- cartilage«
- surgical procedure«
- amount«
- nih«
- tendon«
- oar«
- late teen«
- lining«
- lipid«
- physical therapy«
- groin«
- abnormality«
- limited success«
- dairy product«
- main stage«
- curvature«
- family history«
- foot«
- fetus«
- life expectancy«
- nervous system«
- enlargement«
- types«
- neuron«
- viii«
- common form«
- counseling«
- treatment«
- web page«
- urine«
- adolescence«
- compression«
- clinical trial«
- medical care«
- drug administration«
- injection«
- deficiency«
- thirty«
- membrane«
- mother«
- forehead«
- newsletter«
- study«
- wrist«
- ankle«
- beta«
- jaw«
- hand«
- skeleton«
- alpha«
- adulthood«
- stance«
- seizure«
- pneumonia«
- form«
- trunk«
- features«
- throat«
- muscle«
- tissue«
- cure«
- molecule«
- bout«
- pregnancy«
- alteration«
- overview«
- onset«
- porphyria«
- polygenic disorder«
- polygenic disease«
- pachyderma«
- otosclerosis«
- osteosclerosis congenita«
- osteopetrosis«
- oligodontia«
- oligodactyly«
- nevoid elephantiasis«
- nanism«
- muscular dystrophy«
- monogenic disorder«
- monogenic disease«
- milk intolerance«
- marble bones disease«
- maple syrup urine disease«
- lactose intolerance«
- lactase deficiency«
- juvenile amaurotic idiocy«
- inborn error of metabolism«
- ichthyosis«
- hyperbetalipoproteinemia«
- hepatolenticular degeneration«
- dystrophy«
- congenital pancytopenia«
- congenital megacolon«
- congenital afibrinogenemia«
- chondrodystrophy«
- branched chain ketoaciduria«
- autosomal recessive disease«
- autosomal recessive defect«
- autosomal dominant disorder«
- autosomal dominant disease«
- achondroplasty«
- achondroplasia«
- abetalipoproteinemia«
- xerodermia«
- xeroderma«
- von Recklinghausen's disease«
- tyrosinemia«
- thrombasthenia«
- thalassemia«
- thalassaemia«
- sickle-cell disease«
- sickle-cell anemia«
- sickle-cell anaemia«
- severe combined immunodeficiency disease«
- severe combined immunodeficiency«
- pycnodysostosis«
- pseudohypertrophic dystrophy«
- phenylketonuria«
- pancreatic fibrosis«
- osteogenesis imperfecta«
- oculopharyngeal muscular dystrophy«
- neurofibromatosis«
- myotonic muscular dystrophy«
- myotonic dystrophy«
- myotonia atrophica«
- mucoviscidosis«
- malignant hyperthermia«
- lysinemia«
- limb-girdle muscular dystrophy«
- infantile amaurotic idiocy«
galactosemia, fibrocystic disease of the pancreas, familial hypercholesterolemia, drepanocytic anemia, drepanocytic anaemia, distal muscular dystrophy, diabetes, cystic fibrosis, crescent-cell anemia, crescent-cell anaemia, Hurler's syndrome, Hurler's disease, Hunter syndrome, Wilson's disease, Spielmeyer-Vogt disease, McArdle's disease, Hirschsprung's disease, Fanconi's anemia, Fanconi's anaemia, Albers-Schonberg disease, Werdnig-Hoffman disease, Tay-Sachs disease, Tay-Sachs, Steinert's disease, Sachs disease, SCID, PKU, Niemann-Pick disease, Mediterranean anemia, Mediterranean anaemia, Marfan's syndrome, Huntington's disease, Huntington's chorea, Gaucher's disease, Duchenne's muscular dystrophy, Becker muscular dystrophy,
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