Laryngeal Adductor Paralysis disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

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Aliases & Classifications for Laryngeal Adductor Paralysis

MalaCards integrated aliases for Laryngeal Adductor Paralysis:

Name: Laryngeal Adductor Paralysis ⁵⁷ ¹³

Vocal Cord Dysfunction, Adductor Type ⁵⁷

Lap ⁵⁷

Characteristics:

OMIM:

⁵⁷

Inheritance:
autosomal dominant

HPO:

³²

laryngeal adductor paralysis:
Inheritance autosomal dominant inheritance

External Ids:

OMIM ⁵⁷ 150270

MedGen ⁴² C0396060

SNOMED-CT via HPO ⁶⁹ 263681008 50219008

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Summaries for Laryngeal Adductor Paralysis

MalaCards based summary : Laryngeal Adductor Paralysis, also known as vocal cord dysfunction, adductor type, is related to myhre syndrome and laryngitis. An important gene associated with Laryngeal Adductor Paralysis is LAP (Laryngeal Adductor Paralysis). Affiliated tissues include bone, and related phenotype is hoarse voice.

Description from OMIM: 150270

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Related Diseases for Laryngeal Adductor Paralysis

Diseases related to Laryngeal Adductor Paralysis via text searches within MalaCards or GeneCards Suite gene sharing:

(show all 36)

#	Related Disease	Score
1	myhre syndrome	11.6
2	laryngitis	10.0
3	asthma	9.8
4	leukemia	9.8
5	morbid obesity	9.8
6	ischemia	9.8
7	allergic encephalomyelitis	9.8
8	gastroesophageal reflux	9.7
9	camurati-engelmann disease	9.7
10	hernia, hiatus	9.7
11	systemic lupus erythematosus	9.7
12	thrombophilia due to thrombin defect	9.7
13	insulin-like growth factor i	9.7
14	wilson disease	9.7
15	acute promyelocytic leukemia	9.7
16	spinal stenosis	9.7
17	thrombocytopenia	9.7
18	ulcerative colitis	9.7
19	colitis	9.7
20	inguinal hernia	9.7
21	thrombosis	9.7
22	quadriplegia	9.7
23	obstructive jaundice	9.7
24	beriberi	9.7
25	aggressive periodontitis	9.7
26	lymphangioma	9.7
27	intestinal perforation	9.7
28	cervicitis	9.7
29	breast disease	9.7
30	infertility	9.7
31	periodontitis	9.7
32	appendicitis	9.7
33	lupus erythematosus	9.7
34	hemophilia	9.7
35	fetal and neonatal alloimmune thrombocytopenia	9.7
36	encephalopathy	9.7

Graphical network of the top 20 diseases related to Laryngeal Adductor Paralysis:

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Symptoms & Phenotypes for Laryngeal Adductor Paralysis

Symptoms via clinical synopsis from OMIM:

⁵⁷

Neuro:
laryngeal adductor paralysis

Voice:
congential hoarseness

Clinical features from OMIM:

150270

Human phenotypes related to Laryngeal Adductor Paralysis:

³²

#	Description	HPO Frequency	HPO Source Accession
1	hoarse voice ³²		HP:0001609

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Drugs & Therapeutics for Laryngeal Adductor Paralysis

Search Clinical Trials , NIH Clinical Center for Laryngeal Adductor Paralysis

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Genetic Tests for Laryngeal Adductor Paralysis

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Anatomical Context for Laryngeal Adductor Paralysis

MalaCards organs/tissues related to Laryngeal Adductor Paralysis:

⁴¹

Bone

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Publications for Laryngeal Adductor Paralysis

Articles related to Laryngeal Adductor Paralysis:

#	Title	Authors	Year
1	Laryngeal adductor paralysis treated by vocal cord injection of bone paste; a preliminary investigation. ( 13706299 )	GOFF W.F.	1960

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Genes for Laryngeal Adductor Paralysis

Genes related to Laryngeal Adductor Paralysis (1 elite genes):

- Elite gene

- Cancer Census gene in COSMIC

#	Symbol	Description	Category	Score	Evidence	PubmedIds
1	LAP	Laryngeal Adductor Paralysis	Genetic Locus	58.91	Unconfirmed association ⁵⁷ GeneCards inferred via : Gene name (show sections)

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Variations for Laryngeal Adductor Paralysis

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Expression for Laryngeal Adductor Paralysis

Search GEO for disease gene expression data for Laryngeal Adductor Paralysis.

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Pathways for Laryngeal Adductor Paralysis

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GO Terms for Laryngeal Adductor Paralysis

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Sources for Laryngeal Adductor Paralysis

¹ BioSystems

² BitterDB

³ CDC

⁴ Cell Signaling Technology

⁵ ClinicalTrials

⁶ ClinVar

⁷ CNVD

⁸ Cochrane Library

⁹ Cosmic

¹⁰ dbSNP

¹¹ DGIdb

¹² Disease Ontology

¹³ diseasecard

¹⁴ DiseaseEnhancer

¹⁵ DISEASES

¹⁶ DrugBank

¹⁷ ExPASy

¹⁸ FDA Approved Drugs

¹⁹ FMA

²⁰ GeneAnalytics

²¹ GeneCards

²² GeneGo (Thomson Reuters)

²³ GeneHancer via GeneCards

²⁴ GeneReviews

²⁵ Genetics Home Reference

²⁶ GenomeRNAi

²⁷ GEO DataSets

²⁸ GO

²⁹ GTR

³⁰ HGMD

³¹ HMDB

³² HPO

³³ ICD10

³⁴ ICD10 via Orphanet

³⁵ ICD9CM

³⁶ IUPHAR

³⁷ KEGG

³⁸ LifeMap

³⁹ LncRNADisease

⁴⁰ LOVD

⁴¹ MalaCards

⁴² MedGen

⁴³ MedlinePlus

⁴⁴ MeSH

⁴⁵ MESH via Orphanet

⁴⁶ MGI

⁴⁷ miR2Disease

⁴⁸ NCBI Bookshelf

⁴⁹ NCI

⁵⁰ NCIt

⁵¹ NDF-RT

⁵² NIH Clinical Center

⁵³ NIH Rare Diseases

⁵⁴ NINDS

⁵⁵ Novoseek

⁵⁶ Novus Biologicals

⁵⁷ OMIM

⁵⁸ OMIM via Orphanet

⁵⁹ Orphanet

⁶⁰ PathCards

⁶¹ PharmGKB

⁶² PubMed

⁶³ PubMed Health

⁶⁴ QIAGEN

⁶⁵ R&D Systems

⁶⁶ Reactome

⁶⁷ Sino Biological

⁶⁸ SNOMED-CT

⁶⁹ SNOMED-CT via HPO

⁷⁰ SNOMED-CT via Orphanet

⁷¹ TGDB

⁷² Tocris

⁷³ UMLS

⁷⁴ UMLS via Orphanet

⁷⁵ UniProtKB/Swiss-Prot

⁷⁶ Wikipedia