Nyctalopia
Symptom Information:
Symptom ID: | HPO:0000662 | ||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the eye(HPO:0000478) Abnormal eye physiology(HPO:0012373) Abnormality of vision(HPO:0000504) Nyctalopia(HPO:0000662) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Vitamin related disorders(MedDRA:10047635) Fat soluble vitamin deficiencies and disorders(MedDRA:10016250) Nyctalopia(HPO:0000662) |
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Database Frequency: | 92 / 7739 | ||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 17 | (OMIM:615994) |
Bardet-Biedl syndrome 2 | (OMIM:615981) |
Bardet-Biedl syndrome 3 | (OMIM:600151) |
Bardet-Biedl syndrome 4 | (OMIM:615982) |
Bardet-Biedl syndrome 9 | (OMIM:615986) |
Bothnia retinal dystrophy | (Orphanet:85128) |
Butterfly-shaped pigment dystrophy | (Orphanet:99001) |
CONE-ROD DYSTROPHY 10 | (OMIM:610283) |
CONE-ROD DYSTROPHY 15 | (OMIM:613660) |
CONE-ROD DYSTROPHY 2 | (OMIM:120970) |
CONE-ROD DYSTROPHY 8 | (OMIM:605549) |
Choroideremia | (Orphanet:180) |
Choroideremia - deafness - obesity | (Orphanet:1435) |
Cone dystrophy with supernormal rod response | (Orphanet:209932) |
Cone rod dystrophy | (Orphanet:1872) |
Dent disease type 1 | (Orphanet:93622) |
Fundus albipunctatus | (Orphanet:227796) |
Goldmann-Favre syndrome | (Orphanet:53540) |
Gyrate atrophy of choroid and retina | (Orphanet:414) |
HYPERCAROTENEMIA AND VITAMIN A DEFICIENCY, AUTOSOMAL RECESSIVE | (OMIM:277350) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hyperimmunoglobulinemia D with periodic fever | (Orphanet:343) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Jalili syndrome | (Orphanet:1873) |
Kandori fleck retina | (Orphanet:99179) |
Leber congenital amaurosis 14 | (OMIM:613341) |
Leber congenital amaurosis 15 | (OMIM:613843) |
Leber congenital amaurosis 16 | (OMIM:614186) |
Leber congenital amaurosis 3 | (OMIM:604232) |
Leber congenital amaurosis 4 | (OMIM:604393) |
Leber congenital amaurosis 9 | (OMIM:608553) |
MELAS | (Orphanet:550) |
MRCS syndrome | (Orphanet:263347) |
Microphthalmia - retinitis pigmentosa - foveoschisis - optic disc drusen | (Orphanet:251279) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
NEWFOUNDLAND ROD-CONE DYSTROPHY | (OMIM:607476) |
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B | (OMIM:257270) |
Posterior column ataxia - retinitis pigmentosa | (Orphanet:88628) |
RETINAL CONE DYSTROPHY 3A | (OMIM:610024) |
RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELLABNORMALITIES | (OMIM:616079) |
RETINITIS PIGMENTOSA | (OMIM:268000) |
RETINITIS PIGMENTOSA 1 | (OMIM:180100) |
RETINITIS PIGMENTOSA 13 | (OMIM:600059) |
RETINITIS PIGMENTOSA 18 | (OMIM:601414) |
RETINITIS PIGMENTOSA 19 | (OMIM:601718) |
RETINITIS PIGMENTOSA 2 | (OMIM:312600) |
RETINITIS PIGMENTOSA 20 | (OMIM:613794) |
RETINITIS PIGMENTOSA 25 | (OMIM:602772) |
RETINITIS PIGMENTOSA 27 | (OMIM:613750) |
RETINITIS PIGMENTOSA 28 | (OMIM:606068) |
RETINITIS PIGMENTOSA 30 | (OMIM:607921) |
RETINITIS PIGMENTOSA 33 | (OMIM:610359) |
RETINITIS PIGMENTOSA 35 | (OMIM:610282) |
RETINITIS PIGMENTOSA 37 | (OMIM:611131) |
RETINITIS PIGMENTOSA 38 | (OMIM:613862) |
RETINITIS PIGMENTOSA 4 | (OMIM:613731) |
RETINITIS PIGMENTOSA 41 | (OMIM:612095) |
RETINITIS PIGMENTOSA 43 | (OMIM:613810) |
RETINITIS PIGMENTOSA 45 | (OMIM:613767) |
RETINITIS PIGMENTOSA 47 | (OMIM:613758) |
RETINITIS PIGMENTOSA 50 | (OMIM:613194) |
RETINITIS PIGMENTOSA 54 | (OMIM:613428) |
RETINITIS PIGMENTOSA 56 | (OMIM:613581) |
RETINITIS PIGMENTOSA 58 | (OMIM:613617) |
RETINITIS PIGMENTOSA 6 | (OMIM:312612) |
RETINITIS PIGMENTOSA 61 | (OMIM:614180) |
RETINITIS PIGMENTOSA 62 | (OMIM:614181) |
RETINITIS PIGMENTOSA 63 | (OMIM:614494) |
RETINITIS PIGMENTOSA 66 | (OMIM:615233) |
RETINITIS PIGMENTOSA 68 | (OMIM:615725) |
RETINITIS PIGMENTOSA 70 | (OMIM:615922) |
RETINITIS PIGMENTOSA 9 | (OMIM:180104) |
RETINITIS PIGMENTOSA WITH OR WITHOUT SITUS INVERSUS | (OMIM:615434) |
RETINOPATHY, PERICENTRAL PIGMENTARY, DOMINANT | (OMIM:180210) |
RETINOSCHISIS OF FOVEA | (OMIM:268080) |
Refsum disease | (Orphanet:773) |
Retinal degeneration - nanophthalmos - glaucoma | (Orphanet:1574) |
Retinitis pigmentosa | (Orphanet:791) |
Retinitis pigmentosa 10 | (OMIM:180105) |
Retinitis punctata albescens | (Orphanet:52427) |
Scheie syndrome | (Orphanet:93474) |
Senior-Loken syndrome 8 | (OMIM:616307) |
Short-rib thoracic dysplasia 10 with or without polydactyly | (OMIM:615630) |
Tubular aggregate myopathy | (Orphanet:2593) |
USHER SYNDROME, TYPE IIIA | (OMIM:276902) |
Usher syndrome type 3 | (Orphanet:231183) |
X-linked immunoneurologic disorder | (Orphanet:2571) |
X-linked intellectual disability-retinitis pigmentosa syndrome | (Orphanet:85332) |
Åland Islands eye disease | (Orphanet:178333) |