SLCO2A1 - solute carrier organic anion transporter family member 2A1 Gene

PHOAR2

Pachydermoperiostosis, Autosomal Recessive

Pdp, Autosomal Recessive

Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2

Osteoarthropathy, Hypertrophic, Primary, Autosomal Recessive, Type 2

PHOAD

Pho, Autosomal Dominant

Pachydermoperiostosis, Autosomal Dominant

Pdp, Autosomal Dominant

Ceas

Cranioosteoarthropathy

PHOAR1

Pachydermoperiostosis, Autosomal Recessive

Touraine-Solente-Gole Syndrome

Pho, Autosomal Recessive

Pdp, Autosomal Recessive

Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1

Cranio Osteoarthropathy

Cranio-Osteoarthropathy

Currarino Disease

Currarino Idiopathic Osteoarthropathy

Reginato-Schiapachasse Syndrome

Touraine-Solente-Golé Syndrome

COA

Pachydermoperiostosis Autosomal Recessive

Pdp Autosomal Recessive

Pho Autosomal Recessive

Osteoarthropathy, Hypertrophic, Primary, Autosomal Recessive, Type 1

Osteoarthropathy, Primary Hypertrophic

Reginato Schiapachasse Syndrome

Pachydermoperiostosis

Rosenthal-Kloepfer Syndrome

Pdp

Acromegaloid Changes, Cutis Verticis Gyrata And Corneal Leukoma

Idiopathic Hypertrophic Osteoarthropathy

Primary Hypertrophic Osteoarthropathy

Touraine Solente Gole Syndrome

Touraine-Solente-Gole Syndrome

Pachydermoperiostosis Syndrome

Osteoarthropathy, Primary Hypertrophic

Pachydermoperiostosis Of Nail

Idiopathic Hypertrophic Osteoarthropathy

Pho

Acro-Osteolysis

Osteoarthropathy, Secondary Hypertrophic

Bamberger-Marie Disease

Hpoa - Hypertrophic Pulmonary Osteoarthropathy

Hypertrophic Pulmonary Osteoarthropathy

Marie Bamberger Disease

VMCKD

Cystic Kidney Disease With Ventriculomegaly

Ventriculomegaly-Cystic Kidney Disease

Ventriculomegaly - Cystic Kidney Disease

Congenital Nephrosis-Cerebral Ventriculomegaly Syndrome

SCAR6

Norwegian Infantile Onset Ataxia

Autosomal Recessive Spinocerebellar Ataxia 6

Autosomal Recessive Spinocerebellar Ataxia Type 6

Infantile-Onset Autosomal Recessive Nonprogressive Cerebellar Ataxia

Cerebellar Ataxia, Infantile Nonprogressive, Autosomal Recessive

Spinocerebellar Ataxia Autosomal Recessive 6

Cerebellar Ataxia Infantile Nonprogressive Autosomal Recessive

Potassium Deficiency

Potassium Deficiency Disorder

Hypopotassemia

Potassium

Potassium [K] Deficiency

Hypokalaemic Syndrome

Hypopotassaemia

Hypopotassaemia Syndrome

Hypokalaemic

Potassium Depletion

CHDFIDD

Cdk13-Related Disorder

Cdk13-Related Chdfidd

Cdk13-Related Congenital Heart Defects, Dysmorphic Facial Features, Intellectual Developmental Disorder

Primary Myelofibrosis

Agnogenic Myeloid Metaplasia

Idiopathic Myelofibrosis

Myeloid Metaplasia

Myelofibrosis With Myeloid Metaplasia

Osteomyelofibrosis

Megakaryocytic Myelosclerosis

Myelosclerosis

Chronic Idiopathic Myelofibrosis

Myelofibrosis, Idiopathic

Myelofibrosis With Myeloid Metaplasia, Somatic

Myelofibrosis, Somatic

Aleukemic Myelosis

Bone Marrow Fibrosis

MYELOF

MMM

Agnogenic Myeloid Metaplasia With Myelofibrosis

Ammm

Myelosclerosis With Myeloid Metaplasia

Myelofibrosis Nos

Tuberculosis Of Intestine

Tuberculosis Of Intestines

Heart Failure

Congenital Heart Disease

Heart Diseases

Congenital Heart Defects

Congenital Heart Defect

Heart Malformation

Congenital Anomaly Of Heart

Heart Defect

Heart-Congenital Defect

Congenital Heart Disorder

Heart Defects Congenital

Heart Defects, Congenital

Heart Defects

Heart Disease, Congenital

Disease, Heart, Congenital

Congestive Heart Failure

Osteogenesis Imperfecta Type 4

Osteogenesis Imperfecta Type Iv

OI4

Oi, Type Iv

Osteogenesis Imperfecta With Normal Sclerae

Oi Type Iv

Oi Type 4

Osteogenesis Imperfecta With Normal Sclera

Common Variable Oi With Normal Sclerae

Osteogenesis Imperfecta 4

Oi-Iv

Patent Ductus Arteriosus

PDA1

Pda

Ductus Arteriosus, Patent

Patent Ductus Arteriosus, Susceptibility To

Patent Ductus Botalli

Patency Of The Ductus Arteriosus

Patent Ductus Arteriosus Familial

Ductus Arteriosus Patent

Patent Ductus Arteriosus - Persisting Type