| D007223 |
Infant |
A child between 1 and 23 months of age. |
Infants |
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| D009261 |
Nail-Patella Syndrome |
A syndrome of multiple abnormalities characterized by the absence or hypoplasia of the PATELLA and congenital nail dystrophy. It is a genetically determined autosomal dominant trait. |
Osteo-Onychodysplasia, Hereditary,Osterreicher Syndrome,Pelvic Horn Syndrome,Turner-Kieser Syndrome,Fong Disease,Hereditary Onycho-Osteodysplasia,Hereditary Osteo-Onychodysplasias,Onychoosteodysplasia,Disease, Fong,Hereditary Osteo-Onychodysplasia,Nail Patella Syndrome,Osteo Onychodysplasia, Hereditary,Osteo-Onychodysplasias, Hereditary,Syndrome, Nail-Patella,Syndrome, Osterreicher,Syndrome, Pelvic Horn,Syndrome, Turner-Kieser,Turner Kieser Syndrome |
|
| D011371 |
Progeria |
An abnormal congenital condition, associated with defects in the LAMIN TYPE A gene, which is characterized by premature aging in children, where all the changes of cell senescence occur. It is manifested by premature graying; hair loss; hearing loss (DEAFNESS); cataracts (CATARACT); ARTHRITIS; OSTEOPOROSIS; DIABETES MELLITUS; atrophy of subcutaneous fat; skeletal hypoplasia; elevated urinary HYALURONIC ACID; and accelerated ATHEROSCLEROSIS. Many affected individuals develop malignant tumors, especially SARCOMA. |
Hutchinson-Gilford Syndrome,Hutchinson Gilford Progeria Syndrome,Hutchinson-Gilford Progeria Syndrome,Hutchinson Gilford Syndrome,Hutchinson-Gilford Progeria Syndromes,Progeria Syndrome, Hutchinson-Gilford,Progeria Syndromes, Hutchinson-Gilford |
|
| D006801 |
Humans |
Members of the species Homo sapiens. |
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man |
|
| D000015 |
Abnormalities, Multiple |
Congenital abnormalities that affect more than one organ or body structure. |
Multiple Abnormalities |
|
| D013577 |
Syndrome |
A characteristic symptom complex. |
Symptom Cluster,Cluster, Symptom,Clusters, Symptom,Symptom Clusters,Syndromes |
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