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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	July 8, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **2376 - 2400** of **393515** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
146712	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase like 1	B3GNTL1 Aliases: B3GNT8	Homo sapiens (human)	bronchus cancer bronchus carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer large intestine cancer lung cancer lung carcinoma parapsoriasis psoriasis pustulosis of palm and sole
146760	reticulon 4 receptor like 1	RTN4RL1 Aliases: DKFZp547J144 NGRH2 NgR3 nogo-66 receptor homolog 2	Homo sapiens (human)	acute myeloid leukemia congenital heart disease diabetes mellitus nasopharynx carcinoma type 2 diabetes mellitus
146861	solute carrier family 35 member G3	SLC35G3 Aliases: FLJ40154	Homo sapiens (human)
147007	transmembrane protein 199	TMEM199 Aliases: MGC45714 VMA12 VPH2	Homo sapiens (human)	breast cancer breast carcinoma candidiasis congenital disorder of glycosylation type IIp developmental and epileptic encephalopathy 36 gallbladder disease liver disease steatotic liver disease
147991	dpy-19 like C-mannosyltransferase 3	DPY19L3	Homo sapiens (human)	depressive disorder major depressive disorder melancholic depression obsolete melancholia
148003	galectin 16	LGALS16	Homo sapiens (human)	congestive heart failure diffuse large B-cell lymphoma thyroid adenoma thyroid cancer thyroid gland carcinoma
148641	solute carrier family 35 member F3	SLC35F3 Aliases: FLJ37712	Homo sapiens (human)	acute myeloid leukemia beriberi chronic obstructive pulmonary disease dry beriberi essential hypertension hypertension intracranial aneurysm pellagra thiamine deficiency disease
148738	hemojuvelin BMP co-receptor	HJV Aliases: HFE2A JH RGMC haemojuvelin hemojuvelin repulsive guidance molecule c	Homo sapiens (human)	Duchenne muscular dystrophy Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Kallmann syndrome Meckel syndrome 8 Sheehan syndrome Wilson disease X-linked dilated cardiomyopathy amenorrhea anaplastic astrocytoma androgen insensitivity syndrome arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autosomal recessive polycystic kidney disease azoospermia bacterial infectious disease beta thalassemia breast cancer breast carcinoma cardiomyopathy cerebral infarction cerebrovascular disease childhood cerebral astrocytoma cholestasis chronic kidney disease congenital hypothyroidism congenital nongoitrous hypothyroidism 4 congestive heart failure coronary artery disease diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy endomyocardial fibrosis essential hypertension essential thrombocythemia fibrillary astrocytoma gemistocytic astrocytoma hemochromatosis type 1 hemochromatosis type 2 hemochromatosis type 2A hemochromatosis hepatitis C hepatocellular carcinoma high grade glioma hypertension hypertrophic cardiomyopathy hypogonadism hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism hypothyroidism impotence infertility iron metabolism disease isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency juvenile pilocytic astrocytoma kwashiorkor liver cancer lung squamous cell carcinoma malignant astrocytoma marasmus microcytic anemia middle cerebral artery infarction muscular dystrophy myelodysplastic syndrome myxedema neurogenic arthropathy nutrition disease obesity osteoporosis panhypopituitarism pilocytic astrocytoma polycystic kidney disease 4 porphyria cutanea tarda premature ejaculation protein-energy malnutrition protoplasmic astrocytoma psychologic dyspareunia sick sinus syndrome steatotic liver disease subependymal giant cell astrocytoma thalassemia
148789	beta-1,3-N-acetylgalactosaminyltransferase 2	B3GALNT2 Aliases: MGC39558	Homo sapiens (human)	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bilateral optic nerve hypoplasia blindness breast cancer breast carcinoma cancer cataract cerebral degeneration choreatic disease coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A11 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism depressive disorder developmental coordination disorder distal myopathy dysthymic disorder dystonia embryoma epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis focal epilepsy fundus dystrophy glaucoma hepatocellular carcinoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hypertropia intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia lissencephaly liver cancer major depressive disorder mechanical strabismus melancholic depression meningocele microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia neurotic disorder obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete infantile epileptic encephalopathy obsolete melancholia obstructive hydrocephalus oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy partial motor epilepsy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rippling muscle disease 2 senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly speech disorder stereotypic movement disorder strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type syndromic X-linked intellectual disability type 10 visual epilepsy
149175	mannosidase endo-alpha like	MANEAL Aliases: FLJ31434	Homo sapiens (human)	alternating hemiplegia of childhood autonomic neuropathy central nervous system disease nervous system disease neurodegenerative disease
150223	YdjC chitooligosaccharide deacetylase homolog	YDJC	Homo sapiens (human)	bronchus cancer bronchus carcinoma celiac disease hepatitis B inflammatory bowel disease 1 inflammatory bowel disease lung cancer lung carcinoma parapsoriasis psoriasis pustulosis of palm and sole ulcerative colitis
150763	glycerol-3-phosphate acyltransferase 2, mitochondrial	GPAT2 Aliases: CT123 cancer/testis antigen 123	Homo sapiens (human)	adrenoleukodystrophy breast cancer breast carcinoma cancer melanoma skin melanoma
151056	phospholipase B1	PLB1 Aliases: FLJ30866 PLB	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Balo concentric sclerosis Barrett's esophagus Crohn's colitis Crohn's disease Guillain-Barre syndrome IgA glomerulonephritis IgG4-related disease Krabbe disease Kufor-Rakeb syndrome Marfan syndrome Miller Fisher syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Werner syndrome West Nile fever X-linked chronic granulomatous disease acoustic neuroma acute chest syndrome acute myeloid leukemia acute myocardial infarction adrenoleukodystrophy adult respiratory distress syndrome allergic asthma allergic rhinitis alternating hemiplegia of childhood anaplastic astrocytoma angiomatous meningioma anthrax disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma ataxia telangiectasia atherosclerosis atopic dermatitis autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy autosomal dominant cerebellar ataxia autosomal dominant distal hereditary motor neuronopathy 2 bacterial infectious disease bacterial sepsis basal ganglia disease benign meningioma benign mesothelioma bipolar disorder blepharospasm blood coagulation disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis cardiac arrest cardiovascular system disease cataract central nervous system disease cerebral convexity meningioma cerebral degeneration childhood cerebral astrocytoma chronic ethmoiditis chronic fatigue syndrome chronic granulomatous disease chronic interstitial cystitis chronic kidney disease chronic obstructive pulmonary disease chronic sphenoidal sinusitis clear cell meningioma clonorchiasis colitis colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma complement deficiency coronary artery disease coronary thrombosis cryptococcosis cryptosporidiosis cystic fibrosis depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy dysthymic disorder embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma esophagitis esophagus adenocarcinoma familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia familial nephrotic syndrome fibrillary astrocytoma fibrous meningioma focal hand dystonia focal segmental glomerulosclerosis fragile X-associated tremor/ataxia syndrome gastroduodenal Crohn's disease gastroenteritis gastroesophageal reflux disease gemistocytic astrocytoma glaucoma glomerulonephritis glucose intolerance heart disease hepatitis C hepatocellular carcinoma hereditary spastic paraplegia 35 high grade glioma hyperglycemia ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease intermediate coronary syndrome interstitial cystitis intraorbital meningioma intraventricular meningioma intrinsic asthma islet cell tumor isovaleric acidemia jejunoileitis juvenile pilocytic astrocytoma keratitis keratoconjunctivitis kidney disease large intestine cancer leukemia leukodystrophy lingual-facial-buccal dyskinesia lipoid nephrosis liver cancer liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphangioleiomyomatosis lymphoplasmacyte-rich meningioma macular corneal dystrophy major depressive disorder malignant astrocytoma malignant mesothelioma mastitis melancholic depression membranous glomerulonephritis meningioma meningothelial meningioma microcystic meningioma mood disorder movement disease multiple sclerosis myelitis myocardial infarction narcolepsy nasopharynx carcinoma nephritis nephrosis nephrotic syndrome nervous system disease neuroaxonal dystrophy neuroblastoma neurodegeneration with brain iron accumulation 2a neurodegeneration with brain iron accumulation 2b neurodegeneration with brain iron accumulation 3 neurodegeneration with brain iron accumulation 4 neurodegeneration with brain iron accumulation 5 neurodegeneration with brain iron accumulation 6 neurodegeneration with brain iron accumulation neurodegenerative disease neurotic disorder newborn respiratory distress syndrome nutmeg liver obesity obsolete inherited blood coagulation disease obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia olfactory groove meningioma oral candidiasis osteoarthritis ovarian cancer ovarian carcinoma pantothenate kinase-associated neurodegeneration parapsoriasis parasagittal meningioma patent ductus arteriosus peptic esophagitis pilocytic astrocytoma pituitary adenoma pre-eclampsia prediabetes syndrome primary open angle glaucoma progeria prostate cancer prostate carcinoma protoplasmic astrocytoma psammomatous meningioma psoriasis pulmonary coin lesion pustulosis of palm and sole pyoureter rheumatoid arthritis sarcoidosis schizophrenia secondary Parkinson disease secretory meningioma sick sinus syndrome silent myocardial infarction situs inversus spinal meningioma spinocerebellar ataxia type 2 subependymal giant cell astrocytoma systemic lupus erythematosus thrombophilia transitional meningioma tuberous sclerosis 1 tuberous sclerosis type 2 diabetes mellitus ulcerative colitis uterine corpus cancer uveoparotid fever vascular disease vasculitis vasomotor rhinitis vulvovaginitis
151531	uridine phosphorylase 2	UPP2 Aliases: UDRPASE2 UP2 UPASE2	Homo sapiens (human)	autism spectrum disorder autistic disorder cancer depressive disorder diabetes mellitus major depressive disorder melancholic depression obsolete melancholia squamous cell carcinoma tarsal-carpal coalition syndrome tongue squamous cell carcinoma transitional cell carcinoma type 2 diabetes mellitus
152002	xyloside xylosyltransferase 1	XXYLT1 Aliases: FLJ35155	Homo sapiens (human)	atrial fibrillation bronchus cancer bronchus carcinoma cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma nicotine dependence obesity osteoporosis
152330	contactin 4	CNTN4 Aliases: BIG-2	Homo sapiens (human)	adrenal gland cancer alcohol dependence alcohol use disorder amyotrophic lateral sclerosis type 1 anorexia nervosa autism spectrum disorder autistic disorder autosomal dominant cerebellar ataxia autosomal recessive spinocerebellar ataxia 16 bilateral optic nerve hypoplasia bipolar disorder breast cancer breast carcinoma cancer chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma disease of mental health duodenum cancer epilepsy essential hypertension gallbladder cancer gallbladder carcinoma heart cancer hypertension intellectual disability large intestine cancer learning disability obesity ovarian cancer ovarian carcinoma paraganglioma pheochromocytoma primary open angle glaucoma psychotic disorder schizophrenia small intestine cancer speech disorder trichohepatoenteric syndrome 1 trichohepatoenteric syndrome visual epilepsy
152586	MGAT4 family member D	MGAT4D Aliases: GlcNAcT-I Inhibitory Protein GnT1IP glycosyltransferase 54 domain containing 1 mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase family, member D	Homo sapiens (human)
152831	klotho beta	KLB Aliases: b-Klotho	Homo sapiens (human)	Clostridium difficile colitis allergic rhinitis autosomal dominant hypophosphatemic rickets breast cancer breast carcinoma cancer cartilage-hair hypoplasia diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism embryoma familial hyperlipidemia gestational diabetes hepatocellular carcinoma intrahepatic cholestasis of pregnancy invasive ductal carcinoma irritable bowel syndrome kidney disease kidney failure liver cancer lung cancer lung non-small cell carcinoma neurocirculatory asthenia nodular prostate obesity ovarian disease papillary adenocarcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma prostatic adenoma steatotic liver disease thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma type 2 diabetes mellitus uremia vasomotor rhinitis
153642	arylsulfatase family member K	ARSK Aliases: DKFZp313G1735 TSULF	Homo sapiens (human)	lysosomal storage disease mucopolysaccharidosis
154091	solute carrier family 2 member 12	SLC2A12 Aliases: GLUT12 GLUT8	Homo sapiens (human)	amyloidosis breast cancer cancer congenital hypothyroidism coronary artery disease diabetic ketoacidosis hypothyroidism multiple myeloma myxedema obsolete type 1 diabetes mellitus 9 prostate cancer prostate carcinoma steatotic liver disease type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus
154141	membrane bound O-acyltransferase domain containing 1	MBOAT1 Aliases: LPEAT1 LPLAT14 MGC44669 dJ434O11.1 lysophosphatidylethanolamine acyltransferase 1 lysophospholipid acyltransferase 1 lysophospholipid acyltransferase 14	Homo sapiens (human)	brachydactyly-syndactyly syndrome cholestasis
154516	UDP glucuronosyltransferase 1 family, polypeptide A7C	Ugt1a7c	Rattus norvegicus (Norway rat)	alcoholic pancreatitis cholangiocarcinoma pancreatic cancer type 2 diabetes mellitus
154790	C-type lectin domain family 2 member L	CLEC2L Aliases: FLJ32986	Homo sapiens (human)
154968	O-GlcNAcase	Oga	Rattus norvegicus (Norway rat)	type 2 diabetes mellitus
158326	FRAS1 related extracellular matrix 1	FREM1 Aliases: C9orf143 C9orf145 DKFZp686M16108 FLJ25461 TILRR	Homo sapiens (human)	3p deletion syndrome Angelman syndrome Baraitser-Winter syndrome CAKUT Fraser syndrome 1 Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome NFIA-related disorder Nance-Horan syndrome Potter's syndrome SATB2-associated syndrome Sakati-Nyhan syndrome Smith-Magenis syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome acquired immunodeficiency syndrome anorectal stricture bilateral renal aplasia branchiootic syndrome cardiovascular system disease chromosome 13q14 deletion syndrome chromosome 15q13.3 microdeletion syndrome chromosome 15q24 deletion syndrome chromosome 15q26-qter deletion syndrome chromosome 16p11.2 deletion syndrome, 220-kb chromosome 16p12.2-p11.2 deletion syndrome chromosome 17q12 deletion syndrome chromosome 17q23.1-q23.2 deletion syndrome chromosome 18q deletion syndrome chromosome 1q21.1 deletion syndrome chromosome 1q41-q42 deletion syndrome chromosome 2p16.1-p15 deletion syndrome chromosome 6pter-p24 deletion syndrome chromosome 8q21.11 deletion syndrome chromosome 9p deletion syndrome congenital diaphragmatic hernia craniosynostosis distal 10q deletion syndrome eye disease heart disease hiatus hernia human immunodeficiency virus infectious disease microphthalmia myelofibrosis omphalocele orofaciodigital syndrome I orofaciodigital syndrome X rectal prolapse renal agenesis umbilical hernia

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