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Biological Process
Embryonic Cranial Skeleton Morphogenesis
Diseases Associated With Embryonic Cranial Skeleton Morphogenesis
Disease
Craniofacial Abnormalities
Breast Carcinoma
Intellectual Disability
Osteoarthritis
Heart Defects, Congenital
Cholangiocarcinoma
Colonic Neoplasm
Colorectal Cancer
Liver Cirrhosis, Experimental
Rheumatoid Arthritis
Furlong Syndrome
Lung Neoplasms
Prostatic Neoplasms
Aneurysm, Dissecting
Neoplasm Invasiveness
Neoplasm Metastasis
Autism
Stomach Neoplasms
Tooth Abnormalities
Liver Cirrhosis
Cyclopia
Limb Deformities, Congenital
Mesothelioma, Malignant
Hypertension
Microsatellite Instability
Migraine Disorder
Esophageal Neoplasms
Eye Abnormalities
Aortic Aneurysm
Craniosynostoses
Ovarian Neoplasms
Acth-Secreting Pituitary Adenoma
Cell Transformation, Neoplastic
Urinary Bladder Neoplasms
Uterine Neoplasms
Fractures, Bone
Ventricular Remodeling
Spinal Dysraphism
Neuroblastoma
Carcinoma, Adenoid Cystic
Kidney Disease
Psoriatic Arthritis
Adenocarcinoma
Obesity
Liver Diseases, Parasitic
Tetralogy Of Fallot
Polycystic Ovary Syndrome
Uterine Fibroid
Lung Diseases
Carcinoma
Arthritis, Juvenile
Brachydactyly
Acrocephalosyndactylia
Uremia
Deafness, Autosomal Dominant 23
Deafness, Autosomal Dominant 28
De Lange Syndrome
Dent Disease 1
Dent Disease 2
Dermatitis
Dermatitis, Contact
Diabetic Nephropathy
Digeorge Syndrome
Disease Models, Animal
Dysgnathia Complex
Endocrine System Diseases
Endometrial Neoplasm
Endometriosis
Eosinophilia
Familial Primary Pulmonary Hypertension
Fatigue
Fetal Death
Fibrous Dysplasia, Polyostotic
Gallbladder Neoplasm
Gallstones
Gastrointestinal Stromal Tumors
Goldenhar Syndrome
Growth Disorders
Growth Hormone-Secreting Pituitary Adenoma
Hamartoma Syndrome, Multiple
Hearing Disorders
Hearing Loss, Sensorineural
Hemangiosarcoma
Hemorrhagic Disorders
Hepatitis, Chronic
Hernia, Diaphragmatic
Hernia, Inguinal
Hypereosinophilic Syndrome
Hypoglycemia
Idiopathic Hypogonadotropic Hypogonadism
Immunologic Deficiency Syndromes
Insulin Resistance
Iridogoniodysgenesis, Dominant Type
Jackson-Weiss Syndrome
Kallmann Syndrome
Keratoacanthoma Familial
Lacrimal Apparatus Diseases
Lacrimoauriculodentodigital Syndrome
Leukemia
Leukemia, Lymphoid
Leukemia-Lymphoma, Adult T-Cell
Leukemia, Myeloid
Leukemia, Myelomonocytic, Juvenile
Alcoholic Liver Cirrhosis
Liver Neoplasms
Liver Neoplasms, Experimental
Lymphedema Distichiasis Syndrome
Lymphedema, Hereditary, Ii
Lymphoma
Lymphoma, Large-Cell, Anaplastic
Marfan Syndrome
Medulloblastoma
Microphthalmia, Syndromic 6
Motor Skills Disorders
Mouth Diseases
Mouth Neoplasms
Musculoskeletal Abnormalities
Myopia
Nasopharyngeal Carcinoma
Nasopharyngeal Neoplasm
Neoplasms
Neoplasms, Experimental
Nevus, Sebaceous Of Jadassohn
Noonan Syndrome
Noonan Syndrome 3
Oculocerebrorenal Syndrome
Orofacial Cleft 11
Osseous Heteroplasia, Progressive
Ossification, Heterotopic
Osteosarcoma
Pain
Pancreatic Carcinoma
Cousin Syndrome
Penile Neoplasms
Peters Anomaly
Pfeiffer Type Acrocephalosyndactyly
Phyllodes Tumor
Plagiocephaly, Nonsynostotic
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
Acute Lymphoblastic Leukemia
Prolactinoma
Pseudohypoaldosteronism
Pseudohypoparathyroidism
Pseudohypoparathyroidism Type 1b
Pseudopseudohypoparathyroidism
Pseudoxanthoma Elasticum
Puberty, Precocious
Chronic Obstructive Pulmonary Disease
Recurrence
Respiration Disorders
Respiratory Hypersensitivity
Respiratory System Abnormalities
Retrognathia
Rhabdomyosarcoma, Alveolar
Ring Dermoid Of Cornea
Saethre-Chotzen Syndrome With Eyelid Anomalies
Salivary Gland Neoplasm
Scaphocephaly, Maxillary Retrusion, And Mental Retardation
Schizophrenia
Skin Abnormalities
Skin Diseases
Skin Neoplasms
Spondylarthritis
Stomatognathic System Abnormalities
Drug Dependence
Substance Withdrawal Syndrome
Tachycardia
Thyroid Carcinoma
Timothy Syndrome
Vitamin A Deficiency
Abnormalities, Multiple
Yellow Nail Syndrome
Abortion, Spontaneous
Acromegaly
Acromicric Dysplasia
Adenocarcinoma, Follicular
Lung Adenocarcinoma
Adenoma
Adrenal Gland Neoplasms
Albright's Hereditary Osteodystrophy
Amyotrophic Lateral Sclerosis 1
Anemia, Hypochromic Microcytic
Ankylosis
Anodontia
Anoxia
Antley-Bixler Syndrome Phenotype
Thoracic Aortic Aneurysm
Cardiac Arrhythmia
Asperger Syndrome
Astrocytoma
Atrial Fibrillation
Auditory Neuropathy, Autosomal Dominant, 1
Bipolar Disorder
Bone Diseases
Bone Diseases, Developmental
Bone Neoplasms
Branchiootic Syndrome 3
Branchio-Oto-Renal Syndrome
Brugada Syndrome 3
Burns, Chemical
Cafe-Au-Lait Spots
Carcinogenesis
Hepatocellular Carcinoma
Carcinoma, Non-Small-Cell Lung
Carcinoma, Pancreatic Ductal
Renal Cell Carcinoma
Squamous Cell Carcinoma
Cardiofaciocutaneous Syndrome
Cardiac Hypertrophy
Cardiovascular Abnormalities
Cecal Neoplasms
Charge Syndrome
Chondrosarcoma, Mesenchymal
Chromosome 2q37 Deletion Syndrome
Cleft Lip
Cleidocranial Dysplasia
Cocaine Dependence
Colorectal Neoplasms, Hereditary Nonpolyposis
Congenital Abnormalities
Congenital Disorder Of Glycosylation Type 1a
Copper-Overload Cirrhosis
Costello Syndrome
Craniofacial Dysostosis
Crohn's Disease
Cutis Gyrata Syndrome Of Beare And Stevenson
Related Genes
ALX3
BMP4
CTNNB1
DLX2
FGFR2
GNAS
GRHL2
IRX5
MMP14
MMP16
NODAL
PAX5
PDGFRA
PRRX1
RUNX2
SETD2
SIX1
SIX2
SIX4
SLC39A1
SMAD3
TBX1
TBX15
TFAP2A
TGFBR1
TGFBR2
TWIST1
WDR19
WNT9B
