Symptom Information: Sort according to HPO 

1
(HPO:0000023) Inguinal hernia 181 / 7739
2
(HPO:0000154) Wide mouth 137 / 7739
3
(HPO:0000280) Coarse facial features 189 / 7739
4
(HPO:0000303) Mandibular prognathia 179 / 7739
5
(HPO:0000365) Hearing impairment 539 / 7739
6
(HPO:0000670) Carious teeth 145 / 7739
7
(HPO:0000683) Grayish enamel 2 / 7739
8
(HPO:0000687) Widely spaced teeth 40 / 7739
9
(HPO:0000884) Prominent sternum 11 / 7739
10
(HPO:0000904) Flaring of rib cage 4 / 7739
11
(HPO:0000926) Platyspondyly 150 / 7739
12
(HPO:0000939) Osteoporosis 129 / 7739
13
(HPO:0001223) Pointed proximal second through fifth metacarpals 2 / 7739
14
(HPO:0001388) Joint laxity 117 / 7739
15
(HPO:0001654) Abnormality of the heart valves 49 / 7739
16
(HPO:0002091) Restrictive ventilatory defect 46 / 7739
17
(HPO:0002240) Hepatomegaly 467 / 7739
18
(HPO:0002318) Cervical myelopathy 10 / 7739
19
(HPO:0002650) Scoliosis 705 / 7739
20
(HPO:0002673) Coxa valga 57 / 7739
21
(HPO:0002788) Recurrent upper respiratory tract infections 31 / 7739
22
(HPO:0002808) Kyphosis 289 / 7739
23
(HPO:0002857) Genu valgum 144 / 7739
24
(HPO:0003016) Metaphyseal widening 41 / 7739
25
(HPO:0003049) Ulnar deviation of the wrist 6 / 7739
26
(HPO:0003053) Epiphyseal deformities of tubular bones 2 / 7739
27
(HPO:0003277) Constricted iliac wings 2 / 7739
28
(HPO:0003300) Ovoid vertebral bodies 21 / 7739
29
(HPO:0003307) Hyperlordosis 122 / 7739
30
(HPO:0003308) Cervical subluxation 6 / 7739
31
(HPO:0003311) Hypoplasia of the odontoid process 34 / 7739
32
(HPO:0003521) Disproportionate short-trunk short stature 29 / 7739
33
(HPO:0007759) Opacification of the corneal stroma 77 / 7739
34
(HPO:0007957) Corneal opacity 84 / 7739
35
(HPO:0012069) Keratan sulfate excretion in urine 3 / 7739
36
(HPO:0012070) Chondroitin sulfate excretion in urine 1 / 7739
37
(OMIM) Adult height 82 to 115 cm 1 / 7739
38
(OMIM) Mildly coarse facial features 2 / 7739
39
(OMIM) Hepatomegaly, mild 8 / 7739
40
(OMIM) Normal intelligence 81 / 7739
41
(OMIM) N-acetylgalactosamine-6-sulfatase deficiency in fibroblasts and leukocytes 1 / 7739
42
(OMIM) Keratan sulfate excretion in urine that decreases with age 2 / 7739
43
(OMIM) Chondroitin 6-sulfate excretion in urine 1 / 7739
44
(HPO:0000007) Autosomal recessive inheritance 2538 / 7739
45
(HPO:0003621) Juvenile onset 105 / 7739