Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 12 for Visceral
  1. Heterotaxy syndrome 
    ... isomerism Right isomerism Situs ambiguus Situs ambiguus viscerum Visceral heterotaxy Genetic Testing Registry: Atrioventricular septal defect, partial, ...
    https://medlineplus.gov/genetics/condition/heterotaxy-syndrome - Genetics
  2. Megacystis-microcolon-intestinal hypoperistalsis syndrome 
    ... hypoperistalsis syndrome National Organization for Rare Disorders (NORD) VISCERAL MYOPATHY 1; VSCM1 PubMed Bhagwat PK, Wangler MF. ACTG2 Visceral Myopathy. 2015 Jun 11 [updated 2021 May 6]. ...
    https://medlineplus.gov/...colon-intestinal-hypoperistalsis-syndrome - Genetics
  3. Lysosomal acid lipase deficiency 
    ... condition. Acid esterase deficiency Acid lipase deficiency Familial visceral xanthomatosis Familial xanthomatosis LAL deficiency LIPA deficiency Primary ...
    https://medlineplus.gov/.../lysosomal-acid-lipase-deficiency - Genetics
  4. AMN gene 
    ... amnionless homolog PRO1028 protein amnionless protein amnionless precursor visceral endoderm-specific type 1 transmembrane protein Tests of ...
    https://medlineplus.gov/genetics/gene/amn - Genetics
  5. Intestinal pseudo-obstruction 
    ... CIPO Congenital short bowel syndrome Enteric neuropathy Familial visceral myopathy Familial visceral neuropathy IPO Paralytic ileus Pseudo-obstruction of intestine ...
    https://medlineplus.gov/.../condition/intestinal-pseudo-obstruction - Genetics
  6. Critical congenital heart disease 
    ... Hypoplastic left heart syndrome Genetic Testing Registry: Heterotaxy, visceral, 2, autosomal Genetic Testing Registry: Hypoplastic left heart ... OF THE GREAT ARTERIES, DEXTRO-LOOPED; DTGA HETEROTAXY, VISCERAL, 2, AUTOSOMAL; HTX2 CONGENITAL HEART DEFECTS, MULTIPLE TYPES, ...
    https://medlineplus.gov/.../critical-congenital-heart-disease - Genetics
  7. APOA1 gene 
    ... gene can also cause a condition called familial visceral amyloidosis, which is characterized by an abnormal accumulation ... A-I Tests of APOA1 PubMed AMYLOIDOSIS, FAMILIAL VISCERAL APOLIPOPROTEIN A-I; APOA1 NCBI Gene ClinVar Batal ...
    https://medlineplus.gov/genetics/gene/apoa1 - Genetics
  8. ACVR1 gene 
    ... CL. BMP signaling mediated by ALK2 in the visceral endoderm is necessary for the generation of primordial ...
    https://medlineplus.gov/genetics/gene/acvr1 - Genetics
  9. Niemann-Pick disease 
    ... D Genetic Testing Registry: Sphingomyelin/cholesterol lipidosis Chronic visceral acid sphingomyelinase deficiency Infantile neurovisceral acid sphingomyelinase deficiency ...
    https://medlineplus.gov/genetics/condition/niemann-pick-disease - Genetics
  10. FGA gene 
    ... alpha polypeptide Tests of FGA PubMed AMYLOIDOSIS, FAMILIAL VISCERAL FIBRINOGEN, A ALPHA POLYPEPTIDE; FGA NCBI Gene ClinVar ...
    https://medlineplus.gov/genetics/gene/fga - Genetics
previous · 1 · 2 · next