| Diseases |
Alias |
|
| Isolated Elevated Serum Creatine Phosphokinase Levels |
|
Elevated Serum Cpk
|
Idiopathic Hyperckemia
|
|
Isolated Hyperckemia
|
Elevated Serum Creatine Phosphokinase
|
|
H-Ck
|
Idiopathic Persistent Elevation Of Serum Creatine Kinase
|
|
|
| Hypertension, Essential |
|
Essential Hypertension
|
Hypertension
|
|
High Blood Pressure
|
Hypertension, Essential, Susceptibility To
|
|
Hypertensive Disease
|
Primary Hypertension
|
|
EHT
|
Hypertension, Salt-Sensitive Essential, Susceptibility To
|
|
Hyperpiesia
|
Idiopathic Hypertension
|
|
Hypertensive Disorder
|
Hypertension, Essential, Susceptibility To, 3
|
|
Hypertension, Essential 3
|
Hypertension, Essential, Salt-Sensitive
|
|
Hypertension, Essential, Susceptibility To, 6
|
Hypertension, Essential 6
|
|
Hypertension, Salt-Sensitive Essential
|
Hypertension, Susceptibility To
|
|
Hypertension, Essential, Susceptibility To, 4
|
Hypertension, Essential 4
|
|
Hypertension, Essential, Susceptibility To, 2
|
Hypertension, Essential 2
|
|
Hypertension, Essential, Susceptibility To, 1
|
Hypertension, Essential 1
|
|
Hypertension, Essential, Susceptibility To, 5
|
Hypertension, Essential 5
|
|
Htn
|
Vascular Hypertensive Disorder
|
|
Systemic Primary Arterial Hypertension
|
Hbp - [High Blood Pressure]
|
|
Systemic Arterial Hypertensive Disorder
|
Elevated Blood Pressure
|
|
Arterial Hypertension Nos
|
Hypertension Nos
|
|
Benign Hypertension
|
Systemic Arterial Hypertension
|
|
Systemic Hypertension
|
Artery Htn
|
|
Benign Htn
|
Vascular Htn
|
|
Vascular Hypertension
|
Cholesterol Hypertension
|
|
Cholesterol Htn
|
Idiopathic Htn
|
|
Malignant Hypertension
|
Malignant Htn
|
|
Raised Blood Pressure
|
Cardiovascular Hypertension
|
|
Primary Htn - [Hypertension]
|
High Arterial Tension
|
|
High Blood Pressure Disorder
|
Ht - [Hypertension]
|
|
Htn - [Hypertension]
|
Hypertensive Vascular Disease
|
|
Hypertensive Vascular Degeneration
|
|
|
| Steatocystoma Multiplex |
|
Sebocystomatosis
|
Multiple Sebaceous Cysts
|
|
Multiplex Steatocystoma
|
Sebaceous Cysts, Multiple
|
|
SM
|
|
|
| Bardet-Biedl Syndrome |
|
Bbs
|
Biedl-Bardet Syndrome
|
|
|
| Multicystic Dysplastic Kidney |
|
Multicystic Renal Dysplasia
|
Multicystic Kidney Dysplasia
|
|
Mcdk
|
Multiple Congenital Cysts Of Kidney
|
|
Developmental Multicystic Kidney
|
|
|
| Cystic Fibrosis |
|
Mucoviscidosis
|
CF
|
|
Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis
|
Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis
|
|
Cystic Fibrosis Lung Disease, Modifier Of
|
Cystic Fibrosis Of Pancreas
|
|
Fibrocystic Disease Of Pancreas
|
Cf - [Cystic Fibrosis]
|
|
Cystic Fibrosis Nos
|
Fibrocystic Disease
|
|
Fibrocystic Disease Of The Pancreas
|
Mucoviscidosis Of Pancreas
|
|
Nonproliferative Fibrocystic Disease
|
Pancreatic Cystic Fibrosis
|
|
|
| Meckel Syndrome, Type 1 |
|
Meckel Syndrome
|
Meckel-Gruber Syndrome
|
|
Dysencephalia Splanchnocystica
|
Meckel Syndrome 1
|
|
MKS1
|
Mks
|
|
Gruber Syndrome
|
Meckel-Gruber Syndrome, Type 1
|
|
Mes
|
Dysencephalia Splachnocystica
|
|
Meckel Gruber Syndrome
|
Meckel Syndrome Type 1
|
|
|
| Deafness, Autosomal Recessive 77 |
|
DFNB77
|
Autosomal Recessive Nonsyndromic Deafness 77
|
|
Autosomal Recessive Deafness 77
|
Deafness, Autosomal Recessive, 77
|
|
Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 77
|
Deafness, Autosomal Recessive, Type 77
|
|
|
| Asphyxiating Thoracic Dystrophy |
|
Jeune Thoracic Dystrophy
|
Jeune Syndrome
|
|
Asphyxiating Thoracic Dysplasia
|
Short-Rib Thoracic Dysplasia With Or Without Polydactyly
|
|
Thoracic Pelvic Phalangeal Dystrophy
|
Asphyxiating Thoracic Chondrodystrophy
|
|
Atd
|
Chondroectodermal Dysplasia-Like Syndrome
|
|
Infantile Thoracic Dystrophy
|
Jeune Thoracic Dysplasia
|
|
Thoracic Asphyxiant Dystrophy
|
Thoracic-Pelvic-Phalangeal Dystrophy
|
|
Short-Rib Thoracic Dysplasia Without Polydactyly
|
Asphyxiating Thoracic Dystrophy Of The Newborn
|
|
Asphyxiating Thorax Dystrophy
|
|
|
| Liver Disease |
|
Liver Failure
|
Liver Diseases
|
|
Abnormality Of The Liver
|
Liver Dysfunction
|
|
Disorder Of Liver
|
Hepatic Disorder
|
|
Hepatic Disease
|
Disease Of Bilirubin Metabolism
|
|
Disorder Of Bilirubin Metabolism
|
Liver Decompensation
|
|
Liver Function Failure
|
Hepatic Failure Nos
|
|
Liver Failure Nos
|
End Stage Liver Disease
|
|
Decompensated Liver Failure
|
Decompensation Of Liver Function
|
|
Hepatic Decompensation
|
Hepatic Insufficiency
|
|
Liver Cell Necrosis With Hepatic Failure
|
Liver Insufficiency
|
|
Decompensated Liver Disease
|
End Stage Liver Failure
|
|
Liver Necrosis With Hepatic Failure
|
|
|
| Cystic Kidney Disease |
|
Renal Cyst
|
Simple Renal Cyst
|
|
Kidney Cysts
|
Kidney Diseases, Cystic
|
|
Renal Cysts
|
Kidney Cyst
|
|
Cystic Kidney
|
Congenital Cystic Kidney Disease
|
|
Cystic Kidney Diseases
|
Bosniak 1 Cyst
|
|
|
| Cerebral Aneurysms |
|
Cerebral Aneurysm
|
Cerebral Arterial Aneurysm
|
|
|
| Polycystic Kidney Disease 2 With Or Without Polycystic Liver Disease |
|
Polycystic Kidney Disease 2
|
PKD2
|
|
Polycystic Kidney Disease, Adult, Type Ii
|
Apkd2
|
|
Polycystic Kidney Disease, Type 2
|
Adpkd2
|
|
Adult Polycystic Kidney Disease Type 2
|
Autosomal Dominant Polycystic Kidney Disease 2
|
|
Pkd-2
|
Polycystic Kidney Disease Adult Type Ii
|
|
Polycystic Kidney Type 2 Autosomal Dominant Disease
|
Kidney Disease, Polycystic, Type 2
|
|
|
| Kartagener Syndrome |
|
|
| Nephronophthisis |
|
Medullary Cystic Disease
|
Medullary Cystic Kidney
|
|
Nph
|
Nphp
|
|
Kidney Disease, Cystic, Medullary
|
|
|
| Primary Ciliary Dyskinesia |
|
Immotile Cilia Syndrome
|
Kartagener Syndrome
|
|
Dextrocardia Bronchiectasis And Sinusitis
|
Pcd
|
|
Ciliary Motility Disorders
|
Ciliary Motility Disorder
|
|
Immotile Ciliary Syndrome
|
Ciliary Dyskinesia Primary
|
|
Ics
|
Polynesian Bronchiectasis
|
|
Dextrocardia-Bronchiectasis-Sinusitis Syndrome
|
Immotile Cilia Syndrome, Kartagener Type
|
|
Primary Ciliary Dyskinesia And Situs Inversus
|
Primary Ciliary Dyskinesia, Kartagener Type
|
|
Siewert Syndrome
|
Dyskinesia, Ciliary, Primary
|
|
|
| Hemangioma |
|
|
| Cerebral Arterial Disease |
|
Cerebral Arterial Diseases
|
|
|
| Deafness, Autosomal Recessive 66 |
|
DFNB66
|
Autosomal Recessive Nonsyndromic Deafness 66
|
|
Autosomal Recessive Deafness 66
|
Deafness, Autosomal Recessive, 66
|
|
Deafness, Autosomal Recessive, Type 66
|
|
|
| Nephronophthisis 1 |
|
NPHP1
|
Nephronophthisis, Familial Juvenile
|
|
Nph1
|
Nephronophthisis 1, Juvenile
|
|
Juvenile Nephronophthisis 1
|
Familial Juvenile Nephronophthisis 1
|
|
Nephronophthisis, Type 1
|
|
|
| End Stage Renal Disease |
|
End Stage Renal Failure
|
End-Stage Kidney Disease
|
|
Kidney Failure, Chronic
|
Chronic Kidney Disease Stage 5
|
|
|
| Oligohydramnios |
|
Oligohydramnios - Delivered
|
Antepartum Oligohydramnios
|
|
Delivered Oligohydramnios
|
Oligohydramnios, Antepartum Condition Or Complication
|
|
Deficient Liquor
|
Oligohydramnios, Unspecified Trimester
|
|
Reduced Liquor Volume
|
|
|
| Kidney Disease |
|
Renal Failure
|
Kidney Failure
|
|
Kidney Diseases
|
Nephropathy
|
|
Abnormality Of The Kidney
|
Impaired Renal Function Disease
|
|
Renal Anomaly
|
Kidney Dysfunction
|
|
Renal Disease
|
Nephropathies
|
|
Renal Failure Adverse Event
|
Abnormal Renal Function
|
|
|
| Polycystic Kidney Disease, Infantile Severe, With Tuberous Sclerosis |
|
PKDTS
|
Tuberous Sclerosis/Polycystic Kidney Disease Contiguous Gene Syndrome
|
|
Polycystic Kidneys, Severe Infantile With Tuberous Sclerosis
|
Chromosome 16p13.3 Deletion Syndrome, Distal
|
|
Tuberous Sclerosis Polycystic Kidney Disease Contiguous Gene Syndrome
|
Autosomal Dominant Polycystic Kidney Disease Type 1 With Tuberous Sclerosis
|
|
Tsc2/Pkd1 Contiguous Gene Syndrome
|
|
|
| Renal Dysplasia, Cystic |
|
CYSRD
|
Renal Dysplasia, Cystic, Susceptibility To
|
|
Diffuse Cystic Renal Dysplasia
|
Renal Dysplasia Diffuse Cystic
|
|
Cystic Renal Dysplasia
|
Susceptibility To Cystic Renal Dysplasia
|
|
Dysplasia, Renal, Cystic, Susceptibility To
|
Multicystic Dysplastic Kidney
|
|
|
| Intracranial Berry Aneurysm |
|
Familial Aneurysmal Subarachnoid Hemorrhage
|
Familial Berry Aneurysm
|
|
Familial Intracranial Saccular Aneurysm
|
Saccular Cerebral Aneurysm
|
|
Aneurysm, Intracranial Berry
|
Aneurysmal Subarachnoid Hemorrhage
|
|
Aneurysm, Intracranial Berry, 1
|
|
|
| Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a |
|
Multiple Pterygium Syndrome, Autosomal Dominant
|
CPSFS1A
|
|
Contractures, Pterygia, And Spondylocarpostarsal Fusion Syndrome 1a
|
Autosomal Dominant Disease
|
|
Contractures, Pterygia, And Variable Skeletal Fusions Syndrome 1a
|
Cpskf1a
|
|
Pterygium Syndrome, Multiple
|
Autosomal Dominant
|
|
Arthrogryposis, Distal, Type 8, Formerly
|
Da8, Formerly
|
|
Autosomal Dominant Multiple Pterygium Syndrome
|
Distal Arthrogryposis Type 8
|
|
Arthrogryposis, Distal, Type 8
|
Da8
|
|
Pterygium Syndrome, Multiple, Autosomal Dominant
|
Autosomal Dominant Disorder
|
|
|
| Autosomal Genetic Disease |
|
Autosomal Hereditary Disorder
|
|
|
| Joubert Syndrome 1 |
|
Joubert Syndrome
|
Jbts
|
|
Cerebellooculorenal Syndrome 1
|
JBTS1
|
|
Joubert-Boltshauser Syndrome
|
Cerebelloparenchymal Disorder Iv
|
|
Cpd4
|
Cors1
|
|
Joubert Syndrome And Related Disorders
|
Jsrd
|
|
Familial Aplasia Of The Vermis
|
Joubert Syndrome Related Disorders
|
|
Js
|
Cerebellar Vermis Agenesis
|
|
Cerebelloparenchymal Disorder 4
|
Agenesis Of Cerebellar Vermis
|
|
Cerebello-Oculo-Renal Syndrome
|
Cors
|
|
Joubert-Bolthauser Syndrome
|
Cpd Iv
|
|
Classic Joubert Syndrome
|
Joubert Syndrome Type A
|
|
Pure Joubert Syndrome
|
Cerebello-Oculo-Renal Syndrome 1
|
|
Joubert Syndrome-1
|
Joubert Syndrome, Type 1
|
|
Joubert'S Syndrome
|
|
|
| Fundus Dystrophy |
|
Retinal Dystrophy
|
Retinal Dystrophies
|
|
Dystrophy, Retinal
|
|
|
| Orthostatic Intolerance |
|
Mitral Valve Prolapse
|
Neurocirculatory Asthenia
|
|
Mitral Valve Prolapse Syndrome
|
Irritable Heart
|
|
Systolic Click-Murmur Syndrome
|
Soldiers Heart
|
|
Cardiovascular Malfunction Arising From Mental Factors
|
Cardiovascular Neurosis
|
|
Da Costa'S Syndrome
|
Krishaber'S Disease
|
|
Barlow'S Syndrome
|
Floppy Mitral Valve
|
|
Mitral Leaflet Syndrome
|
Myxomatous Mitral Valve Prolapse
|
|
Postural Orthostatic Tachycardia Syndrome Due To Net Deficiency
|
Familial Orthostatic Tachycardia Due To Norepinephrine Transporter Deficiency
|
|
Orthostatic Intolerance Due To Net Deficiency
|
Pots Due To Net Deficiency
|
|
OI
|
Intolerance, Orthostatic
|
|
Mitral Valve Prolapse, Familial, X-Linked
|
Ballooning Mitral Valve
|
|
Barlow Syndrome
|
Flail Mitral Leaflet
|
|
Myxomatous Mitral Valve
|
Mitral Valve Prolapse-Click Syndrome
|
|
Prolapsing Mitral Valve Leaflet Syndrome
|
Billowing Mitral Valve Leaflet
|
|
Posterior Mitral Leaflet Deformity
|
Ballooning Posterior Leaflet Syndrome
|
|
Blue Valve Syndrome
|
Floppy Mitral Valve Syndrome
|
|
Mitral Valvular Prolapse
|
Systolic Click Syndrome
|
|
|
| Polycystic Kidney Disease 1 With Or Without Polycystic Liver Disease |
|
Polycystic Kidney Disease 1
|
PKD1
|
|
Adpkd
|
Polycystic Kidney Disease, Adult, Type I
|
|
Apkd1
|
Potter Type Iii Polycystic Kidney Disease
|
|
Polycystic Kidney Disease, Adult
|
Potter Type Iii Polycystic Kidney Disease, Formerly
|
|
Polycystic Kidney Disease, Type 1
|
Adpkd1
|
|
Adult Polycystic Kidney Disease Type 1
|
Autosomal Dominant Polycystic Kidney Disease 1
|
|
Pkd-1
|
Polycystic Kidney Disease Adult
|
|
Polycystic Kidney Disease Type I
|
Polycystic Kidneys
|
|
Polycystic Kidney Disease, Adult Type I
|
Polycystic Kidney Type 1 Autosomal Dominant Disease
|
|
Kidney Disease, Polycystic, Type 1
|
Polycystic Kidney, Autosomal Dominant
|
|
Polycystic Kidney, Type 1 Autosomal Dominant Disease
|
Polycystic Kidney Diseases
|
|
|
| Tuberous Sclerosis |
|
Tuberous Sclerosis Syndrome
|
Bourneville'S Disease
|
|
Epiloia
|
Cerebral Sclerosis
|
|
Tuberose Sclerosis
|
Tuberous Sclerosis 1
|
|
Bourneville Disease
|
Bourneville Phakomatosis
|
|
Pringle'S Disease
|
|
|
| Situs Inversus |
|
Situs Inversus Viscerum
|
Laterality Sequence
|
|
Complete Transposition
|
Siv
|
|
|
| Polycystic Kidney Disease 4 With Or Without Polycystic Liver Disease |
|
Autosomal Recessive Polycystic Kidney Disease
|
Arpkd
|
|
Polycystic Kidney Disease, Autosomal Recessive
|
Polycystic Kidney And Hepatic Disease 1
|
|
Pkhd1
|
PKD4
|
|
Polycystic Kidney Disease 4 With Or Without Hepatic Disease
|
Polycystic Kidney Disease, Infantile, Type I
|
|
Polycystic Kidney Disease, Infantile Type
|
Polycystic Kidney, Autosomal Recessive
|
|
Pkd3, Formerly
|
Polycystic Kidney Disease 4, With Or Without Hepatic Disease
|
|
Arpkd/Chf
|
Ar-Pkd
|
|
Polycystic Kidney Disease 4, With Or Without Polycystic Liver Disease
|
Infantile Polycystic Kidney Disease Type I
|
|
Pkd3
|
Kidney, Polycystic, Disease, Type 4, With/Without Hepatic Disease
|
|
Polycystic Kidney Disease 3, Autosomal Dominant
|
|
|
| Chronic Kidney Disease |
|
Chronic Renal Disease
|
Chronic Kidney Failure
|
|
Ckd
|
Chronic Renal Failure
|
|
Kidney Failure, Chronic
|
Chronic Renal Failure Syndrome
|
|
Crf
|
Renal Failure - Chronic
|
|
Renal Failure Chronic
|
Chronic Kidney Diseases
|
|
Chronic Kidney Disease Stage 5
|
Ckd - [Chronic Kidney Disease]
|
|
Crf - [Chronic Renal Failure]
|
Chronic Kidney Impairment
|
|
Chronic Renal Impairment
|
Chronic Kidney Shutdown
|
|
Chronic Hypoxic Kidney Failure
|
Chronic Kidney Collapse
|
|
Chronic Renal Insufficiency
|
Chronic Kidney Toxaemia
|
|
Chronic Kidney Hypofunction
|
Chronic Renal Suppression
|
|
Chronic Renal Failure, Stage 5
|
Ckd - [Chronic Kidney Disease] Stage 5
|
|
End Stage Kidney Failure
|
End Stage Renal Failure
|
|
End Stage Kidney Disease
|
End Stage Renal Disease
|
|
End Stage Chronic Renal Failure
|
Esrf - [End Stage Renal Failure]
|
|
Esrd - [End Stage Renal Diseases]
|
Egfr - [Estimated Glomerular Filtration Rate] < 15 Ml/Min/1.73m²
|
|
|
| Retinitis Pigmentosa |
|
RP
|
Rod-Cone Dystrophy
|
|
Autosomal Recessive Retinitis Pigmentosa
|
Non-Syndromic Retinitis Pigmentosa
|
|
Pericentral Pigmentary Retinopathy
|
Pigmentary Retinopathy
|
|
Tapetoretinal Degeneration
|
Rcd
|
|
Retinitis Pigmentosa Autosomal Recessive
|
ARRP
|
|
Retinitis Pigmentosa, Autosomal Recessive
|
Retinitis Pigmentosa 1
|
|
|
| Polycystic Liver Disease |
|
Autosomal Dominant Polycystic Liver Disease
|
Isolated Polycystic Liver Disease
|
|
Pcld
|
Congenital Cystic Liver Disease
|
|
Congenital Hepatic Cyst
|
Fibrocystic Liver Disease
|
|
Isolated Autosomal Dominant Polycystic Liver Disease
|
Adpcld
|
|
Liver Disease, Polycystic
|
Multiple Cysts Of Liver
|
|
Pld - [Polycystic Liver Disease]
|
Polycystic Liver Disorder
|
|
Polycystic Liver
|
Congenital Polycystic Disease Of Liver
|
|
Congenital Polycystic Liver Disease
|
|
|
| Von Hippel-Lindau Syndrome |
|
Von Hippel-Lindau Disease
|
Vhl
|
|
Vhl Syndrome
|
VHLS
|
|
Von Hippel-Lindau Syndrome, Modifier Of
|
Hippel Lindau Syndrome
|
|
Angiomatosis Retinae
|
Cerebelloretinal Angiomatosis, Familial
|
|
Hippel-Lindau Disease
|
Familial Cerebelloretinal Angiomatosis
|
|
Lindau Disease
|
VHLD
|
|
|
| Creatine Phosphokinase, Elevated Serum |
|
Hyperckemia, Idiopathic
|
Cpk, Elevated Serum
|
|
Hyperckmia
|
HYPCK
|
|
|
| Visceral Heterotaxy |
|
Situs Ambiguus
|
Heterotaxia
|
|
Heterotaxy Syndrome
|
Heterotaxy
|
|
Lateralization Defect
|
Situs Ambiguous
|
|
Left Isomerism
|
Htx
|
|
Ivemark Syndrome
|
Right Isomerism
|
|
Situs Ambiguus Viscerum
|
Incomplete Situs Inversus
|
|
Partial Situs Inversus
|
Heterotaxy, Visceral
|
|
Asplenia Syndrome
|
Bilateral Left-Sidedness
|
|
Polysplenia Syndrome
|
Moller Syndrome
|
|
|
| Renovascular Hypertension |
|
Hypertension, Renovascular
|
Hypertension Renovascular
|
|
|
| Marfan Syndrome |
|
MFS
|
Mfs1
|
|
Marfan'S Syndrome
|
Marfan Syndrome Type 1
|
|
Marfan Syndrome, Type I
|
Mass Phenotype
|
|
Contractural Arachnodactyly
|
Mass Syndrome
|
|
Octd
|
Overlap Connective Tissue Disease
|
|
Marfanoid Hypermobility Syndrome
|
Marfan Disease
|
|
|
| Polycystic Kidney Disease 3 With Or Without Polycystic Liver Disease |
|
PKD3
|
Polycystic Kidney Disease, Adult, Type Iii
|
|
Apkd3
|
Polycystic Kidney Disease 3
|
|
Polycystic Kidney Disease, Type 3
|
Polycystic Kidney Disease 3 Without Polycystic Liver Disease
|
|
Polycystic Kidney Disease 3, Autosomal Dominant
|
|
|
| Nephronophthisis 2 |
|
NPHP2
|
Nph2
|
|
Nephronophthisis 2, Infantile
|
Infantile Nephronophthisis 2
|
|
Infantile Nephronophthisis
|
Nephronophthisis, Type 2
|
|
|
| Autosomal Dominant Polycystic Kidney Disease |
|
Polycystic Kidney Disease, Adult Type
|
Adpkd
|
|
Polycystic Kidney Diseases
|
Polycystic Kidney, Autosomal Dominant
|
|
Congenital Biliary Ectasias
|
Polycystic Kidney And Hepatic Disease 1
|
|
Polycystic Kidney Disease, Autosomal Dominant
|
Kidney, Polycystic, Disease, Autosomal Dominant
|
|
Adult Polycystic Kidney Disease
|
Polycystic Kidney, Adult Type
|
|
Apckd - [Autosomal Polycystic Kidney Disease]
|
|
|
| Polycystic Kidney Disease |
|
Polycystic Kidney Diseases
|
Pkd
|
|
Polycystic Renal Disease
|
Kidney Disease, Polycystic
|
|
Polycystic Kidney, Autosomal Dominant
|
|
|
| Chromosome 2q35 Duplication Syndrome |
|
Syndactyly
|
Syndactyly Type 1
|
|
Sdty1
|
Syndactyly, Type I
|
|
Sd1
|
Zygodactyly
|
|
Syndactyly, Type 1, With Or Without Craniosynostosis
|
Non-Syndromic Syndactyly
|
|
Symphalangism
|
Symphalangy
|
|
Webbing Of Digits
|
Syndactyly, Type 1
|
|
|
| Caroli Disease |
|
Caroli Disease Isolated
|
Congenital Polycystic Dilatation Of Intrahepatic Bile Ducts
|
|
Cystic Dilatation Of The Intrahepatic Biliary Tree
|
Caroli Syndrome
|
|
Carolis Disease
|
|
|
| Polycystic Liver Disease 1 With Or Without Kidney Cysts |
|
Polycystic Liver Disease 1
|
PCLD1
|
|
Liver Disease, Polycystic, Type 1
|
Polycystic Liver Disease
|
|
Cyst
|
|
|
