Diseases Associated With Limb Bud Formation
| Disease |
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Craniofacial Abnormalities
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Cleft Lip
|
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Carcinoma, Adenoid Cystic
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Lacrimoauriculodentodigital Syndrome
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Breast Carcinoma
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Salivary Gland Neoplasm
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Antley-Bixler Syndrome Phenotype
|
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Aplasia Of Lacrimal And Salivary Glands
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Arthritis
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Arthritis, Experimental
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Autism Spectrum Disorder
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Burns, Chemical
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Campomelic Dysplasia
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Carcinoma
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Hepatocellular Carcinoma
|
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Cardiovascular Abnormalities
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Cataract
|
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Cholangiocarcinoma
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Chondrosarcoma
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Coloboma
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Craniofacial Dysostosis
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Craniosynostoses
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Cutis Gyrata Syndrome Of Beare And Stevenson
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Digeorge Syndrome
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Edema
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Endometrial Neoplasm
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Epiphyseal Dysplasia, Multiple, With Myopia And Conductive Deafness
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Erythema
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Eye Abnormalities
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Femur Head Necrosis
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Hamartoma Syndrome, Multiple
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Hand Deformities, Congenital
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Hearing Loss, Sensorineural
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Heart Defects, Congenital
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Cyclopia
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Holoprosencephaly 3
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Holt-Oram Syndrome
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Hyaloideoretinal Degeneration Of Wagner
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Hyperplasia
|
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Inflammation
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Intellectual Disability
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Jackson-Weiss Syndrome
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Kallmann Syndrome
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Kniest Dysplasia
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Legg-Calve-Perthes Disease
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Limb Deformities, Congenital
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Liver Cirrhosis
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Liver Cirrhosis, Experimental
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Liver Neoplasms, Experimental
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Lung Neoplasms
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Lymphoma, Mantle-Cell
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Mammary Neoplasms, Animal
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Mammary Neoplasms, Experimental
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Megaepiphyseal Dwarfism
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Melanoma
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Mesothelioma, Malignant
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Microphthalmia, Isolated, With Coloboma 5
|
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Motor Skills Disorders
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Myopia
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Neoplasm Invasiveness
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Osteoarthritis
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Osteoarthritis With Mild Chondrodysplasia
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Osteochondrodysplasias
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Parkinson Disease, Secondary
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Pfeiffer Type Acrocephalosyndactyly
|
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Pierre Robin Syndrome
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Plagiocephaly, Nonsynostotic
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Platyspondylic Lethal Skeletal Dysplasia, Torrance Type
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Prostatic Neoplasms
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Retinal Detachment
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Scaphocephaly, Maxillary Retrusion, And Mental Retardation
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Schizophrenia
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Single Upper Central Incisor
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Skin Abnormalities
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Skin Diseases
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Spinal Dysraphism
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Spondyloepiphyseal Dysplasia, Congenita
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Spondylometaphyseal Dysplasia, Kozlowski Type
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Stickler Syndrome, Type 1
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Stickler Syndrome, Type I, Nonsyndromic Ocular
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Stomach Neoplasms
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Strudwick Syndrome
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Synovitis
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Tetra-Amelia Autosomal Recessive
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Tetralogy Of Fallot
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Tooth Abnormalities
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Truncus Arteriosus, Persistent
|
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22q11 Deletion Syndrome
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Weight Loss
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Abnormalities, Multiple
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Achondrogenesis Type 2
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Acrocephalosyndactylia
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Ankylosis
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Anonychia Congenita
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