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Clinician Mode
Genomic Search
Disease: OMIM
Disease: HPO
Examples Gene:
MT-ND1
,
POLG
, Region:
M:1-1000
Variant:
m.8993T>G
,
1:g.10042757T>C
rs3888511
MSCV_0000006
, ClinVar:
RCV000000015
, Disease:
Leigh syndrome
, Phenotype:
Retinopathy
Hearing Loss Disease Portal
Choose an Disease for the Annotations:
1 614739 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndro... HL:1 HPO:20 G:1 V: 2
2 100800 Achondroplasia... HL:1 HPO:51 G:1 V: 5
3 CN007581 Adult onset sensorineural hearing impairment... HL:0 HPO:0 G:0 V: 0
4 612448 AGE-RELATED HEARING IMPAIRMENT 1... HL:1 HPO:0 G:0 V: 0
5 612976 AGE-RELATED HEARING IMPAIRMENT 2... HL:1 HPO:0 G:0 V: 0
6 300700 Albinism deafness syndrome... HL:1 HPO:13 G:0 V: 0
7 300650 Albinism ocular late onset sensorineural deafness... HL:1 HPO:12 G:0 V: 0
8 103470 Albinism, ocular, with sensorineural deafness... HL:1 HPO:14 G:0 V: 0
9 C1567741 Alport syndrome... HL:0 HPO:0 G:0 V: 0
10 301050 Alport syndrome, X-linked recessive... HL:1 HPO:18 G:2 V: 555
11 203800 Alstrom syndrome... HL:1 HPO:83 G:1 V: 6
12 CN184091 Aminoglycoside response... HL:0 HPO:0 G:0 V: 0
13 580000 Aminoglycoside-induced deafness... HL:1 HPO:1 G:2 V: 6
14 CN167701 Aminoglycoside-induced hearing loss... HL:0 HPO:0 G:0 V: 0
15 610001 Arthrogryposis multiplex with deafness, inguinal hernias, and early death... HL:1 HPO:0 G:0 V: 0
16 108200 Arthrogryposis-like hand anomaly and sensorineural deafness... HL:1 HPO:8 G:0 V: 0
17 301835 Arts syndrome... HL:1 HPO:36 G:1 V: 5
18 616192 Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes melli... HL:1 HPO:0 G:1 V: 1
19 208750 Ataxia, deafness and cardiomyopathy... HL:1 HPO:6 G:0 V: 0
20 108760 Atresia of external auditory canal and conduction deafness... HL:1 HPO:6 G:0 V: 0
21 607554 Atrial fibrillation, familial, 3... HL:1 HPO:5 G:1 V: 5
22 CN230735 Audiologic phenotype and hearing loss... HL:0 HPO:0 G:0 V: 0
23 CN043167 Auditory neuropathy, autosomal recessive, 1... HL:0 HPO:0 G:0 V: 0
24 242150 Autosomal recessive keratitis-ichthyosis-deafness syndrome... HL:1 HPO:14 G:0 V: 0
25 180500 Axenfeld-Rieger syndrome type 1... HL:1 HPO:34 G:1 V: 6
26 602482 Axenfeld-Rieger syndrome type 3... HL:1 HPO:16 G:1 V: 6
27 614583 Baraitser-Winter Syndrome 2... HL:1 HPO:13 G:1 V: 7
28 602522 Bartter syndrome type 4... HL:1 HPO:29 G:1 V: 6
29 261515 Bifunctional peroxisomal enzyme deficiency... HL:1 HPO:56 G:1 V: 5
30 CN007494 Bilateral conductive hearing impairment... HL:0 HPO:0 G:0 V: 0
31 CN007584 Bilateral sensorineural hearing impairment... HL:0 HPO:0 G:0 V: 0
32 CN231094 Bilateral, progressive nonsyndromic sensorineural hearing loss... HL:0 HPO:0 G:0 V: 0
33 253260 Biotinidase deficiency... HL:1 HPO:40 G:0 V: 0
34 612394 Bone fragility with contractures, arterial rupture, and deafness... HL:1 HPO:30 G:1 V: 1
35 602561 Brachydactyly, intraventricular septal defect, and deafness... HL:1 HPO:0 G:0 V: 0
36 613627 BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY, PTOSIS, HEA... HL:1 HPO:17 G:0 V: 0
37 609166 Branchiogenic-deafness syndrome... HL:1 HPO:25 G:0 V: 0
38 602588 Branchiootic syndrome... HL:1 HPO:14 G:1 V: 2
39 608389 Branchiootic syndrome 3... HL:1 HPO:4 G:1 V: 4
40 CN043574 Branchiootorenal Spectrum Disorders... HL:0 HPO:0 G:0 V: 0
41 610896 Branchiootorenal syndrome 2... HL:1 HPO:6 G:1 V: 4
42 610474 Camptodactyly, tall stature, and hearing loss syndrome... HL:1 HPO:14 G:1 V: 2
43 CN069290 Cardiomyopathy and Deafness... HL:0 HPO:0 G:1 V: 1
44 CN036924 Cardiomyopathy and deafness due to tRNA lysine gene mutation... HL:0 HPO:0 G:0 V: 0
45 212710 Cataract ataxia deafness... HL:1 HPO:20 G:0 V: 0
46 116400 Cataract, nuclear total... HL:1 HPO:3 G:1 V: 1
47 601088 Cataracts, congenital, with sensorineural deafness, down syndrome-like facial ap... HL:1 HPO:10 G:1 V: 7
48 616007 Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing ... HL:1 HPO:0 G:1 V: 1
49 212850 Cerebellar ataxia and neurosensory deafness... HL:1 HPO:4 G:0 V: 0
50 601338 Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing ... HL:1 HPO:14 G:1 V: 1
51 604121 Cerebellar ataxia, deafness, and narcolepsy... HL:1 HPO:15 G:1 V: 3
52 CN035937 Charcot-Marie-Tooth disease deafness recessive type... HL:0 HPO:0 G:0 V: 0
53 311070 Charcot-Marie-Tooth disease, X-linked recessive, type 5... HL:1 HPO:41 G:1 V: 5
54 214800 CHARGE association... HL:1 HPO:132 G:2 V: 50
55 CN167202 Childhood onset sensorineural hearing impairment... HL:0 HPO:0 G:0 V: 0
56 604213 Chudley-McCullough syndrome... HL:1 HPO:15 G:1 V: 4
57 609466 Cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing... HL:1 HPO:0 G:0 V: 0
58 303600 Coffin-Lowry syndrome... HL:1 HPO:94 G:1 V: 9
59 CN000378 Conductive hearing impairment... HL:0 HPO:0 G:0 V: 0
60 268315 Cone-rod dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction... HL:1 HPO:0 G:0 V: 0
61 614482 Congenital cataracts, hearing loss, and neurodegeneration... HL:1 HPO:12 G:1 V: 1
62 CN007559 Congenital conductive hearing impairment... HL:0 HPO:0 G:0 V: 0
63 C0339789 Congenital deafness... HL:0 HPO:0 G:0 V: 0
64 CN007507 Congenital sensorineural hearing impairment... HL:0 HPO:0 G:0 V: 0
65 121450 Corneal degeneration, ribbonlike, with deafness... HL:1 HPO:4 G:0 V: 0
66 217400 Corneal dystrophy and perceptive deafness... HL:1 HPO:7 G:1 V: 4
67 122430 Corneal hypesthesia with retinal abnormalities, sensorineural deafness, unusual ... HL:1 HPO:28 G:0 V: 0
68 122880 Craniofacial deafness hand syndrome... HL:1 HPO:18 G:1 V: 1
69 612247 Crouzon syndrome with acanthosis nigricans... HL:1 HPO:26 G:1 V: 1
70 605685 Cutis verticis gyrata, retinitis pigmentosa, and sensorineural deafness... HL:1 HPO:14 G:0 V: 0
71 221320 Deafness conductive ptosis skeletal anomalies... HL:1 HPO:17 G:0 V: 0
72 234580 Deafness enamel hypoplasia nail defects... HL:1 HPO:29 G:0 V: 0
73 221740 Deafness oligodontia syndrome... HL:1 HPO:7 G:0 V: 0
74 125050 Deafness with anhidrotic ectodermal dysplasia... HL:1 HPO:3 G:0 V: 0
75 610706 Deafness with labyrinthine aplasia microtia and microdontia (LAMM)... HL:1 HPO:26 G:1 V: 12
76 124900 Deafness, autosomal dominant 1... HL:1 HPO:5 G:0 V: 0
77 601316 Deafness, autosomal dominant 10... HL:1 HPO:2 G:1 V: 1
78 601317 Deafness, autosomal dominant 11... HL:1 HPO:3 G:1 V: 3
79 601543 Deafness, autosomal dominant 12... HL:1 HPO:2 G:1 V: 10
80 601868 Deafness, autosomal dominant 13... HL:1 HPO:2 G:1 V: 2
81 602459 Deafness, autosomal dominant 15... HL:1 HPO:2 G:1 V: 4
82 603964 Deafness, autosomal dominant 16... HL:1 HPO:2 G:0 V: 0
83 606012 Deafness, autosomal dominant 18... HL:1 HPO:0 G:0 V: 0
84 604717 Deafness, autosomal dominant 20... HL:1 HPO:4 G:1 V: 8
85 607017 Deafness, autosomal dominant 21... HL:1 HPO:0 G:0 V: 0
86 606346 Deafness, autosomal dominant 22... HL:1 HPO:2 G:1 V: 4
87 605192 Deafness, autosomal dominant 23... HL:1 HPO:3 G:1 V: 1
88 606282 Deafness, autosomal dominant 24... HL:1 HPO:0 G:0 V: 0
89 605583 Deafness, autosomal dominant 25... HL:1 HPO:2 G:1 V: 1
90 612431 Deafness, autosomal dominant 27... HL:1 HPO:0 G:0 V: 0
91 608641 Deafness, autosomal dominant 28... HL:1 HPO:3 G:1 V: 2
92 612644 Deafness, autosomal dominant 2b... HL:1 HPO:2 G:1 V: 2
93 606451 Deafness, autosomal dominant 30... HL:1 HPO:0 G:0 V: 0
94 608645 Deafness, autosomal dominant 31... HL:1 HPO:0 G:0 V: 0
95 614211 Deafness, autosomal dominant 33... HL:1 HPO:4 G:0 V: 0
96 606705 Deafness, autosomal dominant 36... HL:1 HPO:2 G:1 V: 3
97 605594 Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1... HL:1 HPO:5 G:0 V: 0
98 601544 Deafness, autosomal dominant 3a... HL:1 HPO:2 G:1 V: 10
99 612643 Deafness, autosomal dominant 3b... HL:1 HPO:2 G:1 V: 2
100 600652 Deafness, autosomal dominant 4... HL:1 HPO:2 G:1 V: 6
101 616357 DEAFNESS, AUTOSOMAL DOMINANT 40... HL:1 HPO:0 G:1 V: 2
102 608224 Deafness, autosomal dominant 41... HL:1 HPO:2 G:1 V: 2
103 608394 Deafness, autosomal dominant 43... HL:1 HPO:0 G:0 V: 0
104 607453 Deafness, autosomal dominant 44... HL:1 HPO:2 G:0 V: 0
105 608652 Deafness, autosomal dominant 47... HL:1 HPO:0 G:0 V: 0
106 607841 Deafness, autosomal dominant 48... HL:1 HPO:2 G:1 V: 5
107 608372 Deafness, autosomal dominant 49... HL:1 HPO:4 G:0 V: 0
108 614614 Deafness, autosomal dominant 4b... HL:1 HPO:1 G:1 V: 1
109 600994 Deafness, autosomal dominant 5... HL:1 HPO:2 G:1 V: 1
110 613074 Deafness, autosomal dominant 50... HL:1 HPO:3 G:1 V: 2
111 613558 Deafness, autosomal dominant 51... HL:1 HPO:2 G:0 V: 0
112 607683 Deafness, autosomal dominant 52... HL:1 HPO:1 G:0 V: 0
113 615649 Deafness, autosomal dominant 54... HL:1 HPO:0 G:0 V: 0
114 615629 Deafness, autosomal dominant 56... HL:1 HPO:0 G:1 V: 2
115 615654 Deafness, autosomal dominant 58... HL:1 HPO:0 G:0 V: 0
116 612642 Deafness, autosomal dominant 59... HL:1 HPO:0 G:0 V: 0
117 614152 Deafness, autosomal dominant 64... HL:1 HPO:3 G:1 V: 1
118 616044 Deafness, autosomal dominant 65... HL:1 HPO:0 G:1 V: 1
119 616340 DEAFNESS, AUTOSOMAL DOMINANT 67... HL:1 HPO:0 G:0 V: 0
120 601412 Deafness, autosomal dominant 7... HL:1 HPO:2 G:0 V: 0
121 601369 Deafness, autosomal dominant 9... HL:1 HPO:8 G:1 V: 9
122 603622 Deafness, autosomal dominant nonsyndromic sensorineural 17... HL:1 HPO:3 G:1 V: 2
123 C2931767 Deafness, autosomal dominant nonsyndromic sensorineural 22... HL:0 HPO:0 G:0 V: 0
124 C2931768 Deafness, autosomal dominant nonsyndromic sensorineural 23... HL:0 HPO:0 G:0 V: 0
125 C2931769 Deafness, autosomal dominant nonsyndromic sensorineural 24... HL:0 HPO:0 G:0 V: 0
126 609965 Deafness, autosomal dominant nonsyndromic sensorineural 53... HL:1 HPO:0 G:0 V: 0
127 C3148751 Deafness, autosomal dominant, with peripheral neuropathy... HL:0 HPO:0 G:1 V: 1
128 607197 Deafness, autosomal recessive... HL:1 HPO:0 G:1 V: 2
129 615837 Deafness, autosomal recessive 101... HL:1 HPO:0 G:1 V: 1
130 615974 Deafness, autosomal recessive 102... HL:1 HPO:0 G:1 V: 1
131 616042 Deafness, autosomal recessive 103... HL:1 HPO:0 G:1 V: 1
132 601386 Deafness, autosomal recessive 12... HL:1 HPO:4 G:2 V: 10
133 603098 Deafness, autosomal recessive 13... HL:1 HPO:0 G:0 V: 0
134 603678 Deafness, autosomal recessive 14... HL:1 HPO:0 G:0 V: 0
135 601869 Deafness, autosomal recessive 15... HL:1 HPO:3 G:1 V: 6
136 603720 Deafness, autosomal recessive 16... HL:1 HPO:2 G:1 V: 15
137 603010 Deafness, autosomal recessive 17... HL:1 HPO:0 G:0 V: 0
138 602092 Deafness, autosomal recessive 18... HL:1 HPO:2 G:1 V: 2
139 614945 Deafness, autosomal recessive 18b... HL:1 HPO:1 G:1 V: 2
140 220290 Deafness, autosomal recessive 1A... HL:1 HPO:4 G:1 V: 67
141 612645 Deafness, autosomal recessive 1b... HL:1 HPO:2 G:1 V: 1
142 600060 Deafness, autosomal recessive 2... HL:1 HPO:5 G:1 V: 3
143 604060 Deafness, autosomal recessive 20... HL:1 HPO:1 G:0 V: 0
144 603629 Deafness, autosomal recessive 21... HL:1 HPO:2 G:0 V: 0
145 607039 Deafness, autosomal recessive 22... HL:1 HPO:2 G:1 V: 6
146 609533 Deafness, autosomal recessive 23... HL:1 HPO:4 G:2 V: 4
147 611022 Deafness, autosomal recessive 24... HL:1 HPO:3 G:1 V: 3
148 613285 Deafness, autosomal recessive 25... HL:1 HPO:2 G:1 V: 4
149 605428 Deafness, autosomal recessive 26... HL:1 HPO:0 G:0 V: 0
150 605818 Deafness, autosomal recessive 27... HL:1 HPO:0 G:0 V: 0
151 609823 Deafness, autosomal recessive 28... HL:1 HPO:3 G:1 V: 8
152 614035 Deafness, autosomal recessive 29... HL:1 HPO:2 G:1 V: 6
153 600316 Deafness, autosomal recessive 3... HL:1 HPO:2 G:1 V: 18
154 607101 Deafness, autosomal recessive 30... HL:1 HPO:2 G:1 V: 1
155 607084 Deafness, autosomal recessive 31... HL:1 HPO:2 G:1 V: 2
156 608653 Deafness, autosomal recessive 32... HL:1 HPO:0 G:0 V: 0
157 607239 Deafness, autosomal recessive 33... HL:1 HPO:0 G:0 V: 0
158 608565 Deafness, autosomal recessive 35... HL:1 HPO:2 G:1 V: 6
159 609006 Deafness, autosomal recessive 36, with or without vestibular involvement... HL:1 HPO:3 G:0 V: 0
160 C3502293 Deafness, autosomal recessive 36, without vestibular involvement... HL:0 HPO:0 G:0 V: 0
161 607821 Deafness, autosomal recessive 37... HL:1 HPO:3 G:1 V: 3
162 608219 Deafness, autosomal recessive 38... HL:1 HPO:2 G:0 V: 0
163 608265 Deafness, autosomal recessive 39... HL:1 HPO:2 G:1 V: 1
164 608264 Deafness, autosomal recessive 40... HL:1 HPO:2 G:0 V: 0
165 609646 Deafness, autosomal recessive 42... HL:1 HPO:4 G:1 V: 3
166 610154 Deafness, autosomal recessive 44... HL:1 HPO:2 G:1 V: 1
167 612433 Deafness, autosomal recessive 45... HL:1 HPO:0 G:0 V: 0
168 609647 Deafness, autosomal recessive 46... HL:1 HPO:3 G:0 V: 0
169 609439 Deafness, autosomal recessive 48... HL:1 HPO:3 G:1 V: 3
170 610153 Deafness, autosomal recessive 49... HL:1 HPO:2 G:1 V: 1
171 600792 Deafness, autosomal recessive 5... HL:1 HPO:2 G:0 V: 0
172 609941 Deafness, autosomal recessive 51... HL:1 HPO:2 G:0 V: 0
173 609706 Deafness, autosomal recessive 53... HL:1 HPO:2 G:1 V: 1
174 609952 Deafness, autosomal recessive 55... HL:1 HPO:0 G:0 V: 0
175 610220 Deafness, autosomal recessive 59... HL:1 HPO:2 G:1 V: 3
176 600971 Deafness, autosomal recessive 6... HL:1 HPO:3 G:1 V: 6
177 613865 Deafness, autosomal recessive 61... HL:1 HPO:2 G:1 V: 4
178 610143 Deafness, autosomal recessive 62... HL:1 HPO:2 G:0 V: 0
179 611451 Deafness, autosomal recessive 63... HL:1 HPO:2 G:1 V: 5
180 610248 Deafness, autosomal recessive 65... HL:1 HPO:3 G:0 V: 0
181 610212 Deafness, autosomal recessive 66... HL:1 HPO:0 G:0 V: 0
182 610265 Deafness, autosomal recessive 67... HL:1 HPO:3 G:1 V: 2
183 610419 Deafness, autosomal recessive 68... HL:1 HPO:3 G:0 V: 0
184 600974 Deafness, autosomal recessive 7... HL:1 HPO:2 G:1 V: 9
185 614934 Deafness, autosomal recessive 70... HL:1 HPO:1 G:1 V: 1
186 612789 Deafness, autosomal recessive 71... HL:1 HPO:0 G:0 V: 0
187 613718 Deafness, autosomal recessive 74... HL:1 HPO:1 G:1 V: 2
188 615540 Deafness, autosomal recessive 76... HL:1 HPO:0 G:1 V: 1
189 613079 Deafness, autosomal recessive 77... HL:1 HPO:2 G:1 V: 7
190 613307 Deafness, autosomal recessive 79... HL:1 HPO:2 G:1 V: 5
191 605316 Deafness, autosomal recessive 8... HL:1 HPO:0 G:1 V: 15
192 601072 Deafness, autosomal recessive 8... HL:1 HPO:3 G:1 V: 15
193 614129 Deafness, autosomal recessive 81... HL:1 HPO:8 G:1 V: 3
194 613685 Deafness, autosomal recessive 83... HL:1 HPO:0 G:0 V: 0
195 613391 Deafness, autosomal recessive 84... HL:1 HPO:5 G:1 V: 2
196 614944 Deafness, autosomal recessive 84b... HL:1 HPO:2 G:1 V: 1
197 613392 Deafness, autosomal recessive 85... HL:1 HPO:0 G:0 V: 0
198 614617 Deafness, autosomal recessive 86... HL:1 HPO:1 G:1 V: 3
199 615429 Deafness, autosomal recessive 88... HL:1 HPO:0 G:1 V: 1
200 613916 Deafness, autosomal recessive 89... HL:1 HPO:1 G:1 V: 2
201 601071 Deafness, autosomal recessive 9... HL:1 HPO:4 G:1 V: 109
202 613453 Deafness, autosomal recessive 91... HL:1 HPO:2 G:1 V: 1
203 614899 Deafness, autosomal recessive 93... HL:1 HPO:1 G:0 V: 0
204 614414 Deafness, autosomal recessive 96... HL:1 HPO:1 G:0 V: 0
205 614861 Deafness, autosomal recessive 98... HL:1 HPO:1 G:0 V: 0
206 300719 Deafness, cataract, retinitis pigmentosa, and sperm abnormalities... HL:1 HPO:6 G:0 V: 0
207 221200 Deafness, cochlear, with myopia and intellectual impairment... HL:1 HPO:7 G:1 V: 3
208 124490 Deafness, conductive stapedial, with ear malformation and facial palsy... HL:1 HPO:10 G:0 V: 0
209 221300 Deafness, conductive, with malformed external ear... HL:1 HPO:13 G:0 V: 0
210 C1866053 Deafness, congenital heart defects, and posterior embryotoxon... HL:0 HPO:0 G:1 V: 1
211 220300 Deafness, congenital, and familial myoclonic epilepsy... HL:1 HPO:3 G:0 V: 0
212 124480 Deafness, congenital, and onychodystrophy, autosomal dominant... HL:1 HPO:12 G:0 V: 0
213 220900 Deafness, congenital, with total albinism... HL:1 HPO:5 G:0 V: 0
214 221350 Deafness, congenital, with vitiligo and achalasia... HL:1 HPO:9 G:0 V: 0
215 C2673761 Deafness, digenic, GJB2/GJB3... HL:0 HPO:0 G:2 V: 3
216 C2673760 Deafness, digenic, GJB2/GJB6... HL:0 HPO:0 G:2 V: 2
217 304590 Deafness, high-frequency sensorineural, X-linked... HL:1 HPO:0 G:1 V: 6
218 304500 Deafness, high-frequency sensorineural, X-linked... HL:1 HPO:2 G:1 V: 6
219 124700 Deafness, mid-tone neural... HL:1 HPO:4 G:0 V: 0
220 221500 Deafness, neural, congenital moderate... HL:1 HPO:2 G:0 V: 0
221 221700 Deafness, neural, with atypical atopic dermatitis... HL:1 HPO:4 G:0 V: 0
222 609946 Deafness, neurosensory, autosomal recessive 47... HL:1 HPO:0 G:0 V: 0
223 500008 Deafness, nonsyndromic sensorineural, mitochondrial... HL:1 HPO:0 G:6 V: 18
224 605429 Deafness, nonsyndromic, modifier 1... HL:1 HPO:0 G:0 V: 0
225 601449 Deafness, progressive with stapes fixation... HL:1 HPO:3 G:0 V: 0
226 611102 Deafness, sensorineural, and male infertility... HL:1 HPO:4 G:1 V: 1
227 221745 Deafness, sensorineural, autosomal-mitochondrial type... HL:1 HPO:4 G:0 V: 0
228 124950 Deafness, sensorineural, with peripheral neuropathy and arterial disease... HL:1 HPO:11 G:0 V: 0
229 612097 Deafness, unilateral, with delayed endolymphatic hydrops... HL:1 HPO:3 G:0 V: 0
230 C1421921 Deafness, without vestibular involvement, autosomal dominant... HL:0 HPO:0 G:1 V: 3
231 CN043651 Deafness, X-linked... HL:0 HPO:0 G:0 V: 0
232 304400 Deafness, X-linked 2... HL:1 HPO:5 G:1 V: 16
233 300030 Deafness, X-linked 3... HL:1 HPO:2 G:0 V: 0
234 300066 Deafness, X-linked 4... HL:1 HPO:4 G:1 V: 5
235 300614 Deafness, X-linked 5... HL:1 HPO:7 G:1 V: 15
236 300914 Deafness, X-linked 6... HL:1 HPO:0 G:0 V: 0
237 400043 Deafness, Y-linked 1... HL:1 HPO:3 G:0 V: 0
238 125230 Deafness-craniofacial syndrome... HL:1 HPO:17 G:0 V: 0
239 304350 Deafness-hypogonadism syndrome... HL:1 HPO:0 G:0 V: 0
240 125420 Denticles... HL:1 HPO:4 G:1 V: 1
241 125490 Dentinogenesis imperfecta - Shield's type II... HL:1 HPO:2 G:1 V: 4
242 125500 Dentinogenesis imperfecta - Shield's type III... HL:1 HPO:4 G:1 V: 1
243 600101 DFNA 2 Nonsyndromic Hearing Loss... HL:1 HPO:4 G:1 V: 15
244 CN043589 DFNA 3 Nonsyndromic Hearing Loss and Deafness... HL:0 HPO:0 G:0 V: 0
245 CN184629 DFNA6/14/38 Nonsyndromic Low-Frequency Sensorineural Hearing Loss... HL:0 HPO:0 G:0 V: 0
246 CN118854 DFNB 8/10 Nonsyndromic Hearing Loss and Deafness... HL:0 HPO:0 G:0 V: 0
247 222300 Diabetes mellitus AND insipidus with optic atrophy AND deafness... HL:1 HPO:28 G:1 V: 11
248 125853 Diabetes mellitus type 2... HL:1 HPO:4 G:21 V: 27
249 520000 Diabetes-deafness syndrome maternally transmitted... HL:1 HPO:34 G:3 V: 3
250 605362 Dilated cardiomyopathy 1J... HL:1 HPO:5 G:1 V: 1
251 603133 Dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, an... HL:1 HPO:0 G:0 V: 0
252 607323 Duane-radial ray syndrome... HL:1 HPO:78 G:1 V: 6
253 128980 Earlobes, thickened, with conductive deafness from incudostapedial abnormalities... HL:1 HPO:5 G:0 V: 0
254 224800 Ectodermal dysplasia and neurosensory deafness... HL:1 HPO:15 G:0 V: 0
255 609944 Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial feature... HL:1 HPO:22 G:0 V: 0
256 614557 Ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing lo... HL:1 HPO:21 G:0 V: 0
257 602564 Emphysema, congenital, with deafness, penoscrotal web, and mental retardation... HL:1 HPO:0 G:0 V: 0
258 600791 Enlarged vestibular aqueduct syndrome... HL:1 HPO:4 G:4 V: 67
259 162900 Epidermal nevus... HL:1 HPO:3 G:5 V: 11
260 226950 Epiphyseal dysplasia of femoral head, myopia, and deafness... HL:1 HPO:3 G:0 V: 0
261 132450 Epiphyseal dysplasia, multiple, with myopia and conductive deafness... HL:1 HPO:16 G:1 V: 1
262 153650 Epstein syndrome... HL:1 HPO:13 G:1 V: 3
263 133200 Erythrokeratodermia variabilis... HL:1 HPO:32 G:2 V: 11
264 602556 Facial dysmorphism, cleft palate, hearing loss, and camptodactyly... HL:1 HPO:0 G:0 V: 0
265 191900 Familial amyloid nephropathy with urticaria AND deafness... HL:1 HPO:41 G:1 V: 4
266 604352 Febrile seizures, familial, 4... HL:1 HPO:7 G:1 V: 11
267 153640 Fechtner syndrome... HL:1 HPO:14 G:1 V: 7
268 614524 Fibrochondrogenesis 2... HL:1 HPO:16 G:0 V: 0
269 136600 Friedreich ataxia, so-called, with optic atrophy and sensorineural deafness... HL:1 HPO:5 G:0 V: 0
270 233400 Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance... HL:1 HPO:23 G:1 V: 5
271 CN000341 Hearing impairment... HL:0 HPO:0 G:3 V: 29
272 613290 Hearing loss, cisplatin-induced, susceptibility to... HL:1 HPO:0 G:0 V: 0
273 613035 Hearing loss, noise-induced, susceptibility to... HL:1 HPO:0 G:0 V: 0
274 CN229757 Hearing Loss/Deafness... HL:0 HPO:0 G:0 V: 0
275 C0236038 Hereditary hearing loss and deafness... HL:0 HPO:0 G:0 V: 0
276 129500 Hidrotic ectodermal dysplasia syndrome... HL:1 HPO:37 G:1 V: 3
277 CN004526 High-frequency hearing impairment... HL:0 HPO:0 G:0 V: 0
278 CN001598 High-frequency sensorineural hearing impairment... HL:0 HPO:0 G:0 V: 0
279 235740 Hirschsprung disease with polydactyly, renal agenesis, and deafness... HL:1 HPO:11 G:0 V: 0
280 602782 Histiocytosis-lymphadenopathy plus syndrome... HL:1 HPO:28 G:1 V: 11
281 607748 Hypercholanemia, familial... HL:1 HPO:7 G:2 V: 2
282 144300 HYPERLIPOPROTEINEMIA, TYPE II, AND DEAFNESS... HL:1 HPO:8 G:0 V: 0
283 614187 Hypertelorism, preauricular sinus, punctal pits, and deafness... HL:1 HPO:5 G:0 V: 0
284 146000 Hypochondroplasia... HL:1 HPO:30 G:1 V: 2
285 603463 HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA, AND MIXED-TYPE HEARING LOSS... HL:1 HPO:23 G:0 V: 0
286 602540 Hystrix-like ichthyosis with deafness... HL:1 HPO:14 G:1 V: 1
287 CN007576 Infantile sensorineural hearing impairment... HL:0 HPO:0 G:0 V: 0
288 604229 Irido-corneo-trabecular dysgenesis... HL:1 HPO:12 G:3 V: 8
289 601631 Iridogoniodysgenesis type1... HL:1 HPO:6 G:1 V: 1
290 137600 Iridogoniodysgenesis, dominant type... HL:1 HPO:6 G:1 V: 2
291 147750 IVIC syndrome... HL:1 HPO:33 G:0 V: 0
292 311150 Jensen syndrome... HL:1 HPO:7 G:1 V: 1
293 220400 Jervell and Lange-Nielsen syndrome... HL:1 HPO:6 G:3 V: 10
294 612347 Jervell and Lange-Nielsen syndrome 2... HL:1 HPO:4 G:1 V: 3
295 148210 Keratitis-ichthyosis-deafness syndrome, autosomal dominant... HL:1 HPO:23 G:1 V: 5
296 148350 Keratoderma palmoplantar deafness... HL:1 HPO:5 G:2 V: 4
297 148820 Klein-Waardenberg's syndrome... HL:1 HPO:43 G:1 V: 3
298 149200 Knuckle pads, deafness AND leukonychia syndrome... HL:1 HPO:6 G:1 V: 2
299 149730 Levy-Hollister syndrome... HL:1 HPO:79 G:0 V: 0
300 608154 Lipodystrophy, generalized, with mental retardation, deafness, short stature, an... HL:1 HPO:27 G:0 V: 0
301 192500 Long QT syndrome 1... HL:1 HPO:8 G:3 V: 31
302 613695 Long QT syndrome 5... HL:1 HPO:6 G:1 V: 2
303 CN007520 Low-frequency hearing loss... HL:0 HPO:0 G:0 V: 0
304 C3810445 Low-frequency sensorineural hearing impairment... HL:0 HPO:0 G:0 V: 0
305 600208 Macrothrombocytopenia and progressive sensorineural deafness... HL:1 HPO:11 G:1 V: 1
306 273300 Malignant tumor of testis... HL:1 HPO:7 G:3 V: 3
307 615381 Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome... HL:1 HPO:0 G:1 V: 1
308 300519 Martin-Probst deafness-mental retardation syndrome... HL:1 HPO:44 G:1 V: 1
309 248910 Mastocytosis cutaneous with short stature conductive hearing loss and microtia... HL:1 HPO:36 G:0 V: 0
310 155100 May-Hegglin anomaly... HL:1 HPO:11 G:1 V: 7
311 249270 Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineu... HL:1 HPO:34 G:1 V: 5
312 113650 Melnick-Fraser syndrome... HL:1 HPO:40 G:2 V: 19
313 300844 Mental retardation, X-linked 19... HL:1 HPO:2 G:1 V: 3
314 250420 Metaphyseal dysostosis mental retardation conductive deafness... HL:1 HPO:46 G:0 V: 0
315 257920 Michels syndrome... HL:1 HPO:33 G:1 V: 3
316 156620 Microcephaly deafness syndrome... HL:1 HPO:19 G:0 V: 0
317 612947 Microcephaly, growth retardation, cataract, hearing loss, and unusual appearance... HL:1 HPO:22 G:0 V: 0
318 CN181766 Microtia with or without hearing impairment... HL:0 HPO:0 G:0 V: 0
319 612290 Microtia, hearing impairment, and cleft palate... HL:1 HPO:5 G:1 V: 2
320 CN185904 Mid-frequency hearing loss... HL:0 HPO:0 G:0 V: 0
321 CN007565 Mild conductive hearing impairment... HL:0 HPO:0 G:0 V: 0
322 CN185416 Mild hearing impairment... HL:0 HPO:0 G:0 V: 0
323 CN007555 Mild neurosensory hearing impairment... HL:0 HPO:0 G:0 V: 0
324 CN228811 mild-moderate hearing loss... HL:0 HPO:0 G:0 V: 0
325 C0751651 Mitochondrial diseases... HL:0 HPO:0 G:2 V: 13
326 CN000383 Mixed hearing impairment... HL:0 HPO:0 G:0 V: 0
327 CN185420 Moderate conductive hearing impairment... HL:0 HPO:0 G:0 V: 0
328 CN185417 Moderate hearing impairment... HL:0 HPO:0 G:0 V: 0
329 CN007486 Moderate sensorineural hearing impairment... HL:0 HPO:0 G:0 V: 0
330 304700 Mohr-Tranebjaerg syndrome... HL:1 HPO:19 G:1 V: 4
331 253200 Mucopolysaccharidosis type VI... HL:1 HPO:55 G:1 V: 6
332 602849 Muenke syndrome... HL:1 HPO:32 G:1 V: 1
333 124500 Mutilating keratoderma... HL:1 HPO:14 G:1 V: 1
334 CN073381 MYH9 related disorders... HL:0 HPO:0 G:1 V: 12
335 604363 Myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric diso... HL:1 HPO:0 G:0 V: 0
336 159800 Myoclonus, cerebellar ataxia, and deafness... HL:1 HPO:11 G:0 V: 0
337 613076 Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and... HL:1 HPO:6 G:1 V: 1
338 256120 Nephropathy deafness hyperparathyroidism... HL:1 HPO:12 G:0 V: 0
339 609057 Nephropathy with pretibial epidermolysis bullosa and deafness... HL:1 HPO:8 G:0 V: 0
340 609469 Nephropathy, progressive, with deafness... HL:1 HPO:0 G:0 V: 0
341 256200 Nephrosis deafness urinary tract digital malformation... HL:1 HPO:16 G:0 V: 0
342 603641 Neuroendocrine carcinoma of salivary glands, sensorineural hearing loss, and ena... HL:1 HPO:5 G:0 V: 0
343 214370 Neuropathy, hereditary motor and sensory, with deafness, mental retardation, and... HL:1 HPO:19 G:0 V: 0
344 614116 NEUROPATHY, HEREDITARY SENSORY, TYPE IE... HL:1 HPO:14 G:1 V: 3
345 CN231069 NoiseNot providedinduced hearing loss, susceptibility to, association... HL:0 HPO:0 G:0 V: 0
346 CN043648 Non-syndromic genetic deafness... HL:0 HPO:0 G:1 V: 1
347 C3711374 Nonsyndromic Deafness... HL:0 HPO:0 G:2 V: 2
348 CN043649 Nonsyndromic Hearing Loss and Deafness, Autosomal Dominant... HL:0 HPO:0 G:0 V: 0
349 CN043650 Nonsyndromic Hearing Loss and Deafness, Autosomal Recessive... HL:0 HPO:0 G:0 V: 0
350 C1842137 nonsyndromic sensorineural hearing loss... HL:0 HPO:0 G:0 V: 0
351 C0033074 Old-aged sensorineural hearing impairment... HL:0 HPO:0 G:0 V: 0
352 258650 Optic atrophy polyneuropathy deafness... HL:1 HPO:41 G:0 V: 0
353 165199 Optic atrophy, hearing loss, and peripheral neuropathy, autosomal dominant... HL:1 HPO:6 G:0 V: 0
354 166780 Otofaciocervical syndrome... HL:1 HPO:9 G:0 V: 0
355 215150 Otospondylomegaepiphyseal dysplasia... HL:1 HPO:48 G:1 V: 2
356 CN220453 partial sensorineural deafness... HL:0 HPO:0 G:1 V: 1
357 C1853482 Pear-shaped nose... HL:0 HPO:0 G:0 V: 0
358 C1866731 Pear-shaped vertebrae... HL:0 HPO:0 G:0 V: 0
359 274600 Pendred's syndrome... HL:1 HPO:20 G:3 V: 86
360 614369 Peripheral neuropathy, myopathy, hoarseness, and hearing loss... HL:1 HPO:10 G:1 V: 1
361 614926 Perrault syndrome 2... HL:1 HPO:3 G:1 V: 1
362 615300 Perrault syndrome 4... HL:1 HPO:0 G:3 V: 7
363 171480 Phocomelia-ectrodactyly ear malformation deafness and sinus arrhythmia... HL:1 HPO:40 G:0 V: 0
364 300661 Phosphoribosylpyrophosphate synthetase superactivity... HL:1 HPO:21 G:1 V: 6
365 172500 Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunctio... HL:1 HPO:14 G:0 V: 0
366 CN069313 Pigmentary retinopathy and sensorineural deafness... HL:0 HPO:0 G:1 V: 1
367 262000 Pili torti-deafness syndrome... HL:1 HPO:15 G:1 V: 2
368 612674 Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract... HL:1 HPO:23 G:1 V: 7
369 CN007564 Postlingual sensorineural hearing impairment... HL:0 HPO:0 G:0 V: 0
370 CN000372 Prelingual sensorineural hearing impairment... HL:0 HPO:0 G:0 V: 0
371 CN185419 Profound hearing impairment... HL:0 HPO:0 G:0 V: 0
372 CN167204 Profound sensorineural hearing impairment... HL:0 HPO:0 G:0 V: 0
373 C1861325 Progressive conductive hearing impairment... HL:0 HPO:0 G:0 V: 0
374 C1842138 Progressive hearing impairment... HL:0 HPO:0 G:0 V: 0
375 161900 Progressive hereditary glomerulonephritis without deafness... HL:1 HPO:10 G:0 V: 0
376 CN000381 Progressive sensorineural hearing impairment... HL:0 HPO:0 G:0 V: 0
377 264140 Prune belly syndrome with pulmonic stenosis, mental retardation and deafness... HL:1 HPO:6 G:0 V: 0
378 178651 Pulmonic stenosis and deafness... HL:1 HPO:4 G:0 V: 0
379 267300 Renal tubular acidosis with progressive nerve deafness... HL:1 HPO:4 G:1 V: 1
380 C1864499 Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineur... HL:0 HPO:0 G:1 V: 2
381 613809 Retinitis pigmentosa 39... HL:1 HPO:6 G:2 V: 8
382 614180 Retinitis pigmentosa 61... HL:1 HPO:6 G:1 V: 1
383 268010 Retinitis pigmentosa inversa with deafness... HL:1 HPO:6 G:0 V: 0
384 268020 Retinitis pigmentosa, deafness, mental retardation, and hypogonadism... HL:1 HPO:37 G:0 V: 0
385 300455 Retinitis pigmentosa, X-linked, and sinorespiratory infections, with or without ... HL:1 HPO:8 G:0 V: 0
386 500004 Retinitis pigmentosa-deafness syndrome... HL:1 HPO:1 G:1 V: 1
387 180550 Ring dermoid of cornea... HL:1 HPO:3 G:1 V: 1
388 605249 Sebastian syndrome... HL:1 HPO:9 G:1 V: 4
389 607540 Secretory diarrhea, myopathy, and deafness... HL:1 HPO:0 G:0 V: 0
390 C3501265 Sensorineural deafness with hypertrophic cardiomyopathy... HL:0 HPO:0 G:1 V: 1
391 C2748440 Sensorineural deafness with mild renal dysfunction... HL:0 HPO:0 G:1 V: 2
392 CN000380 Sensorineural hearing impairment... HL:0 HPO:0 G:0 V: 0
393 C0018784 Sensorineural hearing loss... HL:0 HPO:0 G:0 V: 0
394 CN196729 sensorineural hearing loss, late onset... HL:0 HPO:0 G:0 V: 0
395 602340 Sensorineural hearing loss, retinal pigment epithelium lesions, discolored teeth... HL:1 HPO:0 G:0 V: 0
396 612780 SeSAME syndrome... HL:1 HPO:27 G:1 V: 9
397 CN185421 Severe conductive hearing impairment... HL:0 HPO:0 G:0 V: 0
398 C2080707 Severe hearing impairment... HL:0 HPO:0 G:0 V: 0
399 CN228592 Severe hearing loss... HL:0 HPO:0 G:0 V: 0
400 CN007590 Severe sensorineural hearing impairment... HL:0 HPO:0 G:0 V: 0
401 609621 Short QT syndrome 2... HL:1 HPO:5 G:1 V: 1
402 614896 Sinoatrial node dysfunction and deafness... HL:1 HPO:2 G:1 V: 1
403 312910 Spastic paraparesis and deafness... HL:1 HPO:20 G:0 V: 0
404 182690 Spastic paraplegia, sensorineural deafness, mental retardation, and progressive ... HL:1 HPO:18 G:0 V: 0
405 220600 Split-hand/foot malformation 1 with sensorineural hearing loss... HL:1 HPO:8 G:1 V: 1
406 184000 Spondyloepiphyseal dysplasia, myopia, and sensorineural deafness... HL:1 HPO:13 G:0 V: 0
407 609616 Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctate calcificati... HL:1 HPO:26 G:0 V: 0
408 184840 Stickler syndrome, type 3... HL:1 HPO:22 G:1 V: 1
409 187600 Thanatophoric dysplasia type 1... HL:1 HPO:55 G:1 V: 15
410 187601 Thanatophoric dysplasia, type 2... HL:1 HPO:18 G:1 V: 1
411 274205 Thumb, hypoplastic, with choroid coloboma, poorly developed antihelix, and deafn... HL:1 HPO:16 G:0 V: 0
412 275230 Tibia, absence of, with congenital deafness... HL:1 HPO:3 G:0 V: 0
413 107480 Townes syndrome... HL:1 HPO:83 G:1 V: 4
414 CN185902 Transient hearing impairment... HL:0 HPO:0 G:0 V: 0
415 275630 Triglyceride storage disease with ichthyosis... HL:1 HPO:18 G:2 V: 6
416 191200 Tune deafness... HL:1 HPO:2 G:0 V: 0
417 CN221712 Unilateral conductive hearing impairment... HL:0 HPO:0 G:0 V: 0
418 125000 Unilateral deafness... HL:1 HPO:2 G:0 V: 0
419 CN008738 Unilateral deafness... HL:0 HPO:0 G:0 V: 0
420 C0339534 Usher syndrome type 2... HL:0 HPO:0 G:0 V: 0
421 C3148929 Usher syndrome type 2c, GPR98/PDZD digenic... HL:0 HPO:0 G:0 V: 0
422 276900 Usher syndrome, type 1... HL:1 HPO:8 G:1 V: 94
423 C1848638 Usher syndrome, type 1B... HL:0 HPO:0 G:1 V: 9
424 276904 Usher syndrome, type 1C... HL:1 HPO:4 G:1 V: 6
425 601067 Usher syndrome, type 1D... HL:1 HPO:4 G:2 V: 36
426 602097 Usher syndrome, type 1E... HL:1 HPO:4 G:0 V: 0
427 602083 Usher syndrome, type 1F... HL:1 HPO:4 G:2 V: 12
428 606943 Usher syndrome, type 1G... HL:1 HPO:5 G:3 V: 8
429 614869 Usher syndrome, type 1J... HL:1 HPO:5 G:1 V: 1
430 276901 Usher syndrome, type 2A... HL:1 HPO:3 G:3 V: 96
431 605472 Usher syndrome, type 2C... HL:1 HPO:3 G:1 V: 21
432 611383 Usher syndrome, type 2D... HL:1 HPO:4 G:1 V: 3
433 276902 Usher syndrome, type 3... HL:1 HPO:7 G:1 V: 11
434 193500 Waardenburg syndrome type 1... HL:1 HPO:39 G:1 V: 6
435 193510 Waardenburg syndrome type 2A... HL:1 HPO:17 G:1 V: 3
436 277580 Waardenburg syndrome type 4A... HL:1 HPO:20 G:1 V: 3
437 613265 Waardenburg syndrome type 4B... HL:1 HPO:12 G:1 V: 4
438 613266 Waardenburg syndrome type 4C... HL:1 HPO:13 G:1 V: 9
439 277610 Weissenbacher-Zweymuller syndrome... HL:1 HPO:14 G:1 V: 1
440 600965 WFS1-Related Disorders... HL:1 HPO:3 G:1 V: 11
441 CN184630 Wolfram syndrome... HL:0 HPO:0 G:0 V: 0
442 604928 Wolfram syndrome 2... HL:1 HPO:8 G:1 V: 1
443 614296 Wolfram-like syndrome, autosomal dominant... HL:1 HPO:10 G:1 V: 3
444 601706 Yemenite deaf-blind hypopigmentation syndrome... HL:1 HPO:27 G:0 V: 0
Switch to table view
Most Common:
Hearing Loss (D034381)
,
Deafness (D003638)
,
Sensorineural HL (D006319)
,
Waardenburg Syndrome
,
Usher Syndromes
Disease Browser
Parent Node:
Lymphatic Diseases
(D008206)
..Starting node
..
Splenic Diseases
(D013158)
Child Nodes:
........
Heterotaxy Syndrome
(D059446)
7
........
Hypersplenism
(D006971)
1
........
Splenic Infarction
(D013159)
........
Splenic Neoplasms
(D013160)
1
........
Splenic Rupture
(D013161)
1
........
Tuberculosis, Splenic
(D014400)
........
Wandering Spleen
(D050805)
Sister Nodes:
..
Capillary Malformation Of The Lower Lip, Lymphatic Malformation Of Face And Neck, Asymmetry Of Face And Limbs, And Partial/Generalized Overgrowth
(C567763)
..
Histiocytosis
(D015614)
32
..
Lymphadenitis
(D008199)
5
..
Lymphangiectasis
(D008200)
5
..
Lymphangitis
(D008205)
..
Lymphatic Abnormalities
(D044148)
10
..
Lymphedema
(D008209)
21
..
Lymphocele
(D008210)
1
..
Lymphoproliferative Disorders
(D008232)
126
..
Mucocutaneous Lymph Node Syndrome
(D009080)
1
..
Pseudolymphoma
(D019310)
..
Splenic Diseases
(D013158)
17
..
Thymus Hyperplasia
(D013952)
..
Thymus Neoplasms
(D013953)
3
..
Tuberculosis, Lymph Node
(D014388)
1
..
Vasculitis, Lymphocytic, Nodular
(C566008)
Human Disease MESH is developed by
UMLS
.
Further data from
MedGen
,
OMIM
,
CTD
Term ID:
10536
Name:
Splenic Diseases
Definition:
Alternative IDs:
ParentIDs:
MESH:D008206
TreeNumbers:
C15.604.744
Synonyms:
Disease, Splenic |Diseases, Splenic |Splenic Disease
Slim Mappings:
Lymphatic disease
Reference:
MedGen:
D013158
MeSH:
D013158
OMIM:
Genes:
Phenotypes
Disease Causing ClinVar Variants