galloway mowat syndrome | Galloway-Mowat syndrome

Keyword	CPC	PCC	Volume	Score	Length of keyword
galloway mowat syndrome	0.34	0.4	1000	30	23
galloway	1.78	0.3	4362	69	8
mowat	0.07	0.3	7070	38	5
syndrome	1.55	0.3	2081	68	8

Keyword	CPC	PCC	Volume	Score
galloway mowat syndrome	0.1	0.5	7907	23
galloway mowat syndrome icd 10	1.35	0.5	9482	38
galloway mowat syndrome life expectancy	0.6	0.6	515	65
galloway mowat syndrome disease	2	0.2	263	80
mowat wilson syndrome icd 10	0.18	0.3	1448	7
icd 10 code for mowat wilson syndrome	1.71	0.5	5969	97
galloway-mowat syndrome	0.24	0.2	4763	83
moyamoya syndrome icd 10	1.56	0.5	2040	65
segawa syndrome icd 10	1.72	0.1	4358	47
icd 10 code for moyamoya syndrome	0.59	1	1629	2
mowa nosowa icd 10	1.24	0.5	4522	48
moyamoya disease icd 10	0.29	0.1	3075	10
gawat janin icd 10	0.88	0.4	2115	42
segawa syndrom icd 10	0.85	0.5	2276	37
wada mowy icd 10	0.8	0.4	3559	78
gawat napas icd 10	0.12	0.4	9868	76
icd 10 code for mogad	1.87	0.8	2645	95

Search Results related to galloway mowat syndrome on Search Engine

Galloway-Mowat syndrome - About the Disease - Genetic and …
nih.gov

https://rarediseases.info.nih.gov/diseases/65/galloway-mowat-syndrome/

WEBGalloway-Mowat syndrome is a rare, neurodegenerative disorder characterized by various developmental and physical abnormalities. Signs and symptoms may include small head size (microcephaly); developmental delay; seizures; nephrotic syndrome; hiatal hernia; optic atrophy; movement disorders; and intellectual disability.

DA: 65 PA: 35 MOZ Rank: 94

Galloway-Mowat Syndrome - Symptoms, Causes, Treatment
rarediseases.org

https://rarediseases.org/rare-diseases/galloway-mowat-syndrome/

WEBMay 9, 2016 · Disease Overview. Galloway-Mowat syndrome is an extremely rare genetic disorder that is characterized by a variety of physical and developmental abnormalities, particularly neurological abnormalities and early onset progressive kidney disease.

DA: 44 PA: 62 MOZ Rank: 20

Galloway–Mowat syndrome - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/Galloway%E2%80%93Mowat_syndrome

WEBGalloway–Mowat syndrome is a very rare autosomal recessive [1] genetic disorder, consisting of a variety of features including hiatal hernia, microcephaly and nephrotic syndrome. [2] Cause. The exact genetic defect in Galloway–Mowat syndrome is …

DA: 76 PA: 68 MOZ Rank: 65

Orphanet: Galloway-Mowat syndrome
orpha.net

https://www.orpha.net/en/disease/detail/2065

WEBA rare, genetic multisystem disorder characterized by a neurodegenerative disorder associating global developmental delay, progressive microcephaly, and progressive cerebral and cerebellar atrophy with extrapyramidal involvement, progressive optic atrophy, and in many patients early-onset steroid-resistant nephrotic syndrome.

DA: 21 PA: 69 MOZ Rank: 88

GARD Rare Disease Information - Galloway-Mowat syndrome
rarediseases.org

https://rarediseases.org/gard-rare-disease/galloway-mowat-syndrome/

WEBGalloway-Mowat syndrome is a rare, neurodegenerative disorder characterized by various developmental and physical abnormalities. [10780] [10781] Signs and symptoms may include small head size (microcephaly); developmental delay; seizures; nephrotic syndrome; hiatal hernia; optic atrophy; movement disorders; and intellectual disability. …

DA: 59 PA: 93 MOZ Rank: 63

Entry - #251300 - GALLOWAY-MOWAT SYNDROME 1; GAMOS1 …
omim.org

https://www.omim.org/entry/251300

WEBOct 24, 2017 · Galloway-Mowat syndrome is a rare autosomal recessive neurodegenerative disorder characterized by infantile onset of microcephaly and central nervous system abnormalities resulting in severely delayed psychomotor development. Brain imaging shows cerebellar atrophy and sometimes cerebral atrophy.

DA: 52 PA: 7 MOZ Rank: 62

Galloway-Mowat syndrome - Getting a Diagnosis - Genetic and …
nih.gov

https://rarediseases.info.nih.gov/diseases/65/galloway-mowat-syndrome/diagnosis/

WEBGalloway-Mowat syndrome. Other Names: . Galloway syndrome; Microcephaly-hiatus hernia-nephrotic syndrome; Nephrosis-neuronal dysmigration syndromeGalloway syndrome; Microcephaly-hiatus hernia-nephrotic syndrome; Nephrosis-neuronal dysmigration syndrome. Read More . Read Less . About the Disease . Getting a …

DA: 6 PA: 75 MOZ Rank: 90

Galloway-Mowat Syndrome | Hereditary Ocular Diseases
arizona.edu

https://disorders.eyes.arizona.edu/disorders/galloway-mowat-syndrome

WEBClinical Characteristics. Ocular Features: Microphthalmia, hypertelorism, epicanthal folds and ptosis are prominent ocular features. Other manifestations include corneal opacities, cataracts, and optic atrophy. Nystagmus of a roving nature is seen in all individuals and is usually present at birth.

DA: 19 PA: 23 MOZ Rank: 6

Galloway-Mowat Syndrome | Hereditary Ocular Diseases
arizona.edu

https://disorders.eyes.arizona.edu/handouts/galloway-mowat-syndrome

WEBBackground and History: This is a severe inherited condition with extensive malformations and a usually short lifespan. The primary manifestations are developmental delay and kidney disease. Clinical Correlations: Infants have a low birth weight due to intrauterine growth retardation.

DA: 43 PA: 14 MOZ Rank: 48

Galloway-Mowat syndrome - NIH Genetic Testing Registry (GTR) …
nih.gov

https://www.ncbi.nlm.nih.gov/gtr/conditions/C0795949/

WEBGalloway-Mowat syndrome is a rare autosomal recessive neurodegenerative disorder characterized by infantile onset of microcephaly and central nervous system abnormalities resulting in severely delayed psychomotor development. Brain imaging shows cerebellar atrophy and sometimes cerebral atrophy.

DA: 67 PA: 94 MOZ Rank: 31