C1865070 |
SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION
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disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Stomatognathic Diseases; Behavior and Behavior Mechanisms
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Disease or Syndrome
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|
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1 |
C0265269 |
Lacrimoauriculodentodigital syndrome
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disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases
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Disease or Syndrome
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genetic disease
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3 |
C1852406 |
Cutis Gyrata Syndrome of Beare And Stevenson
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disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
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Disease or Syndrome
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genetic disease
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|
1 |
C2936791 |
Antley-Bixler Syndrome, Autosomal Dominant
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disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
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Disease or Syndrome
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genetic disease
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|
1 |
C0175699 |
Saethre-Chotzen Syndrome
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disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
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Disease or Syndrome
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genetic disease; disease of anatomical entity
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|
3 |
C0001193 |
Apert syndrome
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disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
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Congenital Abnormality
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genetic disease; disease of anatomical entity; syndrome
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|
1 |
C0795998 |
JACKSON-WEISS SYNDROME
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disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
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Disease or Syndrome
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genetic disease
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|
1 |
C1510455 |
Acrocephalosyndactylia
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disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
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Congenital Abnormality
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genetic disease; disease of anatomical entity
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|
1 |
C3281247 |
BENT BONE DYSPLASIA SYNDROME
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disease |
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Disease or Syndrome
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disease of anatomical entity
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1 |