PedAM

Pediatric Disease Annotations & Medicines


	progressive muscular atrophy

Disease ID	1378
Disease	progressive muscular atrophy
Definition	A rare, milder form of amyotrophic lateral sclerosis. It is characterized by a slowly progressive clinical course. Signs and symptoms include muscle weakness, atrophy, and fasciculation.
Synonym	atrophies, progressive muscular atrophy, progressive muscular duchenne-aran muscular atrophy muscular atrophies, progressive muscular atrophy, progressive myelopathic muscular atrophy, progressive pma - progressive muscular atrophy prog muscular atrophy progressive muscular atrophies progressive muscular atrophy (disorder) progressive myelopathic muscular atrophy pure progressive muscular atrophy
DOID	DOID:318
UMLS	C0917981
SNOMED-CT	SNOMEDCT_US_2016_09_01:88923002
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:3) C1136085 \| monoclonal gammopathy \| 2 C0022735 \| klinefelter's syndrome \| 1 C0011127 \| pressure sores \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:61) 8106 \| PABPN1 \| DISEASES 10084 \| PQBP1 \| DISEASES 1158 \| CKM \| DISEASES 2091 \| FBL \| DISEASES 2218 \| FKTN \| DISEASES 5341 \| PLEK \| DISEASES 23435 \| TARDBP \| DISEASES 4656 \| MYOG \| DISEASES 4654 \| MYOD1 \| DISEASES 1160 \| CKMT2 \| DISEASES 2521 \| FUS \| DISEASES 967 \| CD63 \| DISEASES 11258 \| DCTN3 \| DISEASES 4001 \| LMNB1 \| DISEASES 59341 \| TRPV4 \| DISEASES 23531 \| MMD \| DISEASES 4854 \| NOTCH3 \| DISEASES 25978 \| CHMP2B \| DISEASES 23095 \| KIF1B \| DISEASES 3931 \| LCAT \| DISEASES 3073 \| HEXA \| DISEASES 6647 \| SOD1 \| DISEASES 761 \| CA3 \| DISEASES 326 \| AIRE \| DISEASES 4131 \| MAP1B \| DISEASES 1152 \| CKB \| DISEASES 1159 \| CKMT1B \| DISEASES 3992 \| FADS1 \| DISEASES 5663 \| PSEN1 \| DISEASES 283 \| ANG \| DISEASES 4624 \| MYH6 \| DISEASES 1778 \| DYNC1H1 \| DISEASES 23299 \| BICD2 \| DISEASES 7415 \| VCP \| DISEASES 1639 \| DCTN1 \| DISEASES 2316 \| FLNA \| DISEASES 959 \| CD40LG \| DISEASES 4593 \| MUSK \| DISEASES 6015 \| RING1 \| DISEASES 367 \| AR \| DISEASES 4758 \| NEU1 \| DISEASES 6311 \| ATXN2 \| DISEASES 1804 \| DPP6 \| DISEASES 3801 \| KIFC3 \| DISEASES 203228 \| C9orf72 \| DISEASES 6606 \| SMN1 \| DISEASES 6607 \| SMN2 \| DISEASES 2737 \| GLI3 \| DISEASES 54664 \| TMEM106B \| DISEASES 4780 \| NFE2L2 \| DISEASES 8291 \| DYSF \| DISEASES 3800 \| KIF5C \| DISEASES 5817 \| PVR \| DISEASES 548596 \| CKMT1A \| DISEASES 5830 \| PEX5 \| DISEASES 400916 \| CHCHD10 \| DISEASES 114907 \| FBXO32 \| DISEASES 4671 \| NAIP \| DISEASES 10687 \| PNMA2 \| DISEASES 5053 \| PAH \| DISEASES 820 \| CAMP \| DISEASES
Locus	(Waiting for update.)

Disease ID	1378
Disease	progressive muscular atrophy
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:1) HP:0012399 \| Bedsore \| 1

Disease ID	1378
Disease	progressive muscular atrophy
Manually Symptom	UMLS \| Name(Total Manually Symptoms:1) C0085084 \| motor neuron disease
Text Mined Symptom	(Waiting for update.)

Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)

All Snps(Total Genotypes:0)
(Waiting for update.)

GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)

GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)

Mapped by lexical matching(Total Items:0)
(Waiting for update.)

Mapped by homologous gene(Total Items:0)
(Waiting for update.)

Chemical(Total Drugs:0)
(Waiting for update.)

FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)

FDA labeling changes(Total Drugs:0)
(Waiting for update.)

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