| proteinaceous extracellular matrix | 0.0279911 | 4.91 | 16 | MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY, KEUTEL SYNDROME, COLE-CARPENTER SYNDROME 1, WEAVER SYNDROME, ?GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES, HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC, SCHWARTZ-JAMPEL SYNDROME, TYPE 1, SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY, HYPOTHYROIDISM, CONGENITAL, DUE TO THYROID DYSGENESIS OR HYPOPLASIA, MELNICK-NEEDLES SYNDROME, ?OSTEOGENESIS IMPERFECTA, TYPE X, URBACH-WIETHE DISEASE, MYHRE SYNDROME, ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED, GELEOPHYSIC DYSPLASIA 1, ACROMICRIC DYSPLASIA | 16 | RAPSN, HSPG2, FLNA, MGP, MUSK, TRPV4, SMAD4, FBN1, SERPINH1, EDA, ADAMTSL2, PAX8, EZH2, IGF2, P4HB, ECM1 |
| extracellular matrix | 0.000881263 | 4.58 | 20 | SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY, KEUTEL SYNDROME, COLE-CARPENTER SYNDROME 1, WEAVER SYNDROME, ?GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES, HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC, SCHWARTZ-JAMPEL SYNDROME, TYPE 1, ACROMICRIC DYSPLASIA, MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY, COSTELLO SYNDROME, CONGENITAL MYOPATHY WITH EXCESS OF MUSCLE SPINDLES, MELNICK-NEEDLES SYNDROME, HYPOPHOSPHATASIA, INFANTILE, ?OSTEOGENESIS IMPERFECTA, TYPE X, URBACH-WIETHE DISEASE, MYHRE SYNDROME, INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL, ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED, GELEOPHYSIC DYSPLASIA 1, HYPOTHYROIDISM, CONGENITAL, DUE TO THYROID DYSGENESIS OR HYPOPLASIA, SIALIDOSIS, TYPE I, SIALIDOSIS, TYPE II | 20 | RAPSN, ALPL, HSPG2, FLNA, MGP, TRPV4, MUSK, ITGA3, SMAD4, FBN1, SERPINH1, EDA, NEU1, ADAMTSL2, PAX8, EZH2, HRAS, IGF2, P4HB, ECM1 |