lessthan40multiplestepaug Computer Vision Project
geneticDisorders
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Classes (215)
3MC_syndrome
3_Methylglutaconic_aciduria
ACROFACIAL_DYSOSTOSIS_1_NAGER_TYPE__AFD1
ACROMICRIC_DYSPLASIA__ACMICD
AGENESIS_OF_CORPUS_CALLOSUM_CARDIAC_OCULAR_AND_GENITAL_SYNDROME__ACOGS
ALAZAMI_SYNDROME__ALAZS
ALPHA_THALASSEMIA_MENTAL_RETARDATION_SYNDROME_X_LINKED__ATRX
ALSTROM_SYNDROME__ALMS
ALZAHRANI_KUWAHARA_SYNDROME__ALKUS
AL_KAISSI_SYNDROME__ALKAS
AL_RAQAD_SYNDROME__ARS
AYME_GRIPP_SYNDROME__AYGRP
Autism_susceptiblity_to
BAINBRIDGE_ROPERS_SYNDROME__BRPS
BASILICATA_AKHTAR_SYNDROME__MRXSBA
BEAULIEU_BOYCOTT_INNES_SYNDROME__BBIS
BECK_FAHRNER_SYNDROME__BEFAHRS
BLEPHAROPHIMOSIS_IMPAIRED_INTELLECTUAL_DEVELOPMENT_SYNDROME__BIS
BLEPHAROPHIMOSIS_PTOSIS_AND_EPICANTHUS_INVERSUS__BPES
BOHRING_OPITZ_SYNDROME__BOPS
BORJESON_FORSSMAN_LEHMANN_SYNDROME__BFLS
BOSCH_BOONSTRA_SCHAAF_OPTIC_ATROPHY_SYNDROME__BBSOAS
BOSMA_ARHINIA_MICROPHTHALMIA_SYNDROME__BAMS
BRANCHIOOCULOFACIAL_SYNDROME__BOFS
BURN_MCKEOWN_SYNDROME__BMKS
Bardet_Biedl_syndrome
CANTU_SYNDROME
CAREY_FINEMAN_ZITER_SYNDROME__CFZS
CDH8
CEBALID_SYNDROME__CEBALID
CEREBELLAR_OCULAR_CRANIOFACIAL_AND_GENITAL_SYNDROME__COFG
CEREBELLOFACIODENTAL_SYNDROME__CFDS
CEREBROCOSTOMANDIBULAR_SYNDROME__CCMS
CHOPS_SYNDROME__CHOPS
CHROMOSOME_22q11_2_DELETION_SYNDROME_DISTAL
CHUNG_JANSEN_SYNDROME__CHUJANS
CLARK_BARAITSER_SYNDROME__CLABARS
CLEFT_PALATE_CARDIAC_DEFECTS_AND_MENTAL_RETARDATION__CPCMR
CLEIDOCRANIAL_DYSPLASIA__CCD
COFFIN_LOWRY_SYNDROME__CLS
COGNITIVE_FUNCTION_1_SOCIAL__CGF1
CONGENITAL_CATARACTS_FACIAL_DYSMORPHISM_AND_NEUROPATHY__CCFDN
CONGENITAL_HEART_DEFECTS_MULTIPLE_TYPES_2__CHTD2
CONGENITAL_HYPOTONIA_EPILEPSY_DEVELOPMENTAL_DELAY_AND_DIGITAL_ANOMALIES__CHEDDA
Cold_induced_sweating_syndrome
Craniosynostosis
DEAFNESS_CATARACT_IMPAIRED_INTELLECTUAL_DEVELOPMENT_AND_POLYNEUROPATHY__DCIDP
DESANTO_SHINAWI_SYNDROME__DESSH
DEVELOPMENTAL_AND_EPILEPTIC_ENCEPHALOPATHY_28__DEE28
DEVELOPMENTAL_AND_EPILEPTIC_ENCEPHALOPATHY_2__DEE2
DEVELOPMENTAL_AND_EPILEPTIC_ENCEPHALOPATHY_4__DEE4
DEVELOPMENTAL_AND_EPILEPTIC_ENCEPHALOPATHY_66__DEE66
DEVELOPMENTAL_AND_EPILEPTIC_ENCEPHALOPATHY_80__DEE80
DEVELOPMENTAL_AND_EPILEPTIC_ENCEPHALOPATHY_83__DEE83
DEVELOPMENTAL_AND_EPILEPTIC_ENCEPHALOPATHY_87__DEE87
DEVELOPMENTAL_DELAY_HYPOTONIA_MUSCULOSKELETAL_DEFECTS_AND_BEHAVIORAL_ABNORMALITIES__DEHMBA
DEVELOPMENTAL_DELAY_IMPAIRED_GROWTH_DYSMORPHIC_FACIES_AND_AXONAL_NEUROPATHY__DIGFAN
DEVELOPMENTAL_DELAY_WITH_OR_WITHOUT_DYSMORPHIC_FACIES_AND_AUTISM__DEDDFA
DEVELOPMENTAL_DELAY_WITH_OR_WITHOUT_INTELLECTUAL_IMPAIRMENT_OR_BEHAVIORAL_ABNORMALITIES__DDIB
DEVELOPMENTAL_DELAY_WITH_VARIABLE_INTELLECTUAL_IMPAIRMENT_AND_BEHAVIORAL_ABNORMALITIES__DDVIBA
DIETS_JONGMANS_SYNDROME__DIJOS
DIGEORGE_SYNDROME__DGS
DOWN_SYNDROME
FACIAL_PALSY_CONGENITAL_WITH_PTOSIS_AND_VELOPHARYNGEAL_DYSFUNCTION__FPVEPD
FBXW7
FG_syndrome
FOCAL_DERMAL_HYPOPLASIA__FDH
FONTAINE_PROGEROID_SYNDROME__FPS
Fraser_syndrome
Frontometaphyseal_dysplasia
GAND_SYNDROME__GAND
GAPO_SYNDROME__GAPOS
GENITOPATELLAR_SYNDROME__GTPTS
GERODERMA_OSTEODYSPLASTICUM__GO
GLASS_SYNDROME__GLASS
GNAI1
Galloway_Mowat_syndrome
H3_3A
H3_3B
H4C5
HARTSFIELD_SYNDROME__HRTFDS
HEART_AND_BRAIN_MALFORMATION_SYNDROME__HBMS
HIATT_NEU_COOPER_NEURODEVELOPMENTAL_SYNDROME__HINCONS
HYPOPARATHYROIDISM_RETARDATION_DYSMORPHISM_SYNDROME__HRDS
HYPOTONIA_ATAXIA_AND_DELAYED_DEVELOPMENT_SYNDROME__HADDS
Hennekam_lymphangiectasia_lymphedema_syndrome
Hermansky_Pudlak_syndrome
Hyper_IgE_recurrent_infection_syndrome
Hypotonia_infantile_with_psychomotor_retardation_and_characteristic_facies
IMPAIRED_INTELLECTUAL_DEVELOPMENT_AND_DISTINCTIVE_FACIAL_FEATURES_WITH_OR_WITHOUT_CARDIAC_DEFECTS__MRFACD
INTELLECTUAL_DEVELOPMENTAL_DISORDER_AUTOSOMAL_DOMINANT_21__MRD21
INTELLECTUAL_DEVELOPMENTAL_DISORDER_AUTOSOMAL_DOMINANT_23__MRD23
INTELLECTUAL_DEVELOPMENTAL_DISORDER_AUTOSOMAL_DOMINANT_26__MRD26
INTELLECTUAL_DEVELOPMENTAL_DISORDER_AUTOSOMAL_DOMINANT_40__MRD40
INTELLECTUAL_DEVELOPMENTAL_DISORDER_AUTOSOMAL_DOMINANT_62__MRD62
INTELLECTUAL_DEVELOPMENTAL_DISORDER_AUTOSOMAL_DOMINANT_6_WITH_OR_WITHOUT_SEIZURES__MRD6
INTELLECTUAL_DEVELOPMENTAL_DISORDER_AUTOSOMAL_DOMINANT_7__MRD7
INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_AUTISTIC_FEATURES_AND_LANGUAGE_DELAY_WITH_OR_WITHOUT_SEIZURES__IDDALDS
INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_CARDIAC_DEFECTS_AND_DYSMORPHIC_FACIES__IDDCDF
INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_DYSMORPHIC_FACIES_AND_BEHAVIORAL_ABNORMALITIES__IDDFBA
INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_DYSMORPHIC_FACIES_AND_PTOSIS__IDDDFP
INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_DYSMORPHIC_FACIES_SEIZURES_AND_DISTAL_LIMB_ANOMALIES__IDDFSDA
INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_SEVERE_SPEECH_AND_AMBULATION_DEFECTS__IDDSSAD
INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_SPEECH_DELAY_AUTISM_AND_DYSMORPHIC_FACIES__IDDSADF
INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_SPEECH_DELAY_DYSMORPHIC_FACIES_AND_T_CELL_ABNORMALITIES__IDDSFTA
INTELLECTUAL_DEVELOPMENTAL_DISORDER_X_LINKED_93__XLID93
INTELLECTUAL_DEVELOPMENTAL_DISORDER_X_LINKED_99_SYNDROMIC_FEMALE_RESTRICTED__MRXS99F
INTELLECTUAL_DEVELOPMENTAL_DISORDER_X_LINKED_SYNDROMIC_BILLUART_TYPE__MRXSBL
INTELLECTUAL_DEVELOPMENTAL_DISORDER_X_LINKED_SYNDROMIC_CABEZAS_TYPE__MRXSC
INTELLECTUAL_DEVELOPMENTAL_DISORDER_X_LINKED_SYNDROMIC_CLAES_JENSEN_TYPE__MRXSCJ
INTELLECTUAL_DEVELOPMENTAL_DISORDER_X_LINKED_SYNDROMIC_HACKMANN_DI_DONATO_TYPE__MRXSHD
INTELLECTUAL_DEVELOPMENTAL_DISORDER_X_LINKED_SYNDROMIC_LUBS_TYPE__MRXSL
INTELLECTUAL_DEVELOPMENTAL_DISORDER_X_LINKED_SYNDROMIC_NASCIMENTO_TYPE__MRXSN
INTELLECTUAL_DEVELOPMENTAL_DISORDER_X_LINKED_SYNDROMIC_SNIJDERS_BLOK_TYPE__MRXSSB
INTELLECTUAL_DEVELOPMENTAL_DISORDER_X_LINKED_SYNDROMIC_SNYDER_ROBINSON_TYPE__MRXSSR
INTELLECTUAL_DEVELOPMENTAL_DISORDER_X_LINKED_SYNDROMIC_TURNER_TYPE__MRXST
INTRAUTERINE_GROWTH_RETARDATION_METAPHYSEAL_DYSPLASIA_ADRENAL_HYPOPLASIA_CONGENITA_GENITAL_ANOMALIES_AND_IMMUNODEFICIENCY__IMAGEI
Immunodeficiency_centromeric_instability_facial_anomalies
JANSEN_DE_VRIES_SYNDROME__JDVS
JOHANSON_BLIZZARD_SYNDROME__JBS
KAUFMAN_OCULOCEREBROFACIAL_SYNDROME__KOS
KDM2B
LARSEN_SYNDROME__LRS
LESSEL_KREIENKAMP_SYNDROME__LESKRES
LIG4_SYNDROME
LUSCAN_LUMISH_SYNDROME__LLS
Leukodystrophy_hypomyelinating
Linear_skin_defects_with_multiple_congenital_anomalies
Long_QT_syndrome
MACROCEPHALY_ACQUIRED_WITH_IMPAIRED_INTELLECTUAL_DEVELOPMENT__MACID
MACROCEPHALY_AUTISM_SYNDROME
MANDIBULOFACIAL_DYSOSTOSIS_GUION_ALMEIDA_TYPE__MFDGA
MANNOSIDOSIS_ALPHA_B_LYSOSOMAL__MANSA
MARSHALL_SMITH_SYNDROME__MRSHSS
MARSHALL_SYNDROME__MRSHS
MEGALENCEPHALY_CAPILLARY_MALFORMATION_POLYMICROGYRIA_SYNDROME__MCAP
MENTAL_RETARDATION_AUTOSOMAL_DOMINANT_57__MRD57
MICROCEPHALIC_OSTEODYSPLASTIC_PRIMORDIAL_DWARFISM_TYPE_II__MOPD2
MICROCEPHALY_WITH_OR_WITHOUT_CHORIORETINOPATHY_LYMPHEDEMA_OR_MENTAL_RETARDATION__MCLMR
MOEBIUS_SYNDROME__MBS
MYHRE_SYNDROME__MYHRS
Meier_Gorlin_syndrome
Microcephaly_growth_restriction_and_increased_sister_chromatid_exchange
Microcephaly_primary
Microphthalmia_syndromic
Multiple_congenital_anomalies_hypotonia_seizures_syndrome
NEURODEVELOPMENTAL_DISORDER_AND_LANGUAGE_DELAY_WITH_OR_WITHOUT_STRUCTURAL_BRAIN_ABNORMALITIES__NEDLBA
NEURODEVELOPMENTAL_DISORDER_WITH_DYSMORPHIC_FACIES_AND_DISTAL_LIMB_ANOMALIES__NEDDFL
NEURODEVELOPMENTAL_DISORDER_WITH_DYSMORPHIC_FACIES_AND_DISTAL_SKELETAL_ANOMALIES__NEDDFSA
NEURODEVELOPMENTAL_DISORDER_WITH_DYSMORPHIC_FACIES_IMPAIRED_SPEECH_AND_HYPOTONIA__NEDDISH
NEURODEVELOPMENTAL_DISORDER_WITH_HEARING_LOSS_SEIZURES_AND_BRAIN_ABNORMALITIES__NEDHSB
NEURODEVELOPMENTAL_DISORDER_WITH_HYPOTONIA_AND_VARIABLE_INTELLECTUAL_AND_BEHAVIORAL_ABNORMALITIES__NEDHIB
NEURODEVELOPMENTAL_DISORDER_WITH_NEONATAL_RESPIRATORY_INSUFFICIENCY_HYPOTONIA_AND_FEEDING_DIFFICULTIES__NEDRIHF
NEURODEVELOPMENTAL_DISORDER_WITH_OR_WITHOUT_HYPERKINETIC_MOVEMENTS_AND_SEIZURES_AUTOSOMAL_DOMINANT__NDHMSD
NEURODEVELOPMENTAL_DISORDER_WITH_SEVERE_MOTOR_IMPAIRMENT_AND_ABSENT_LANGUAGE__NEDMIAL
NEURODEVELOPMENTAL_DISORDER_WITH_SPASTIC_DIPLEGIA_AND_VISUAL_DEFECTS__NEDSDV
NEURODEVELOPMENTAL_DISORDER_WITH_SPEECH_IMPAIRMENT_AND_DYSMORPHIC_FACIES__NEDSID
NEUROFIBROMATOSIS_TYPE_I__NF1
NEUROOCULOCARDIOGENITOURINARY_SYNDROME__NOCGUS
NIJMEGEN_BREAKAGE_SYNDROME__NBS
Noonan_syndrome_like_disorder_with_loose_anagen_hair
OCULODENTODIGITAL_DYSPLASIA__ODDD
OKUR_CHUNG_NEURODEVELOPMENTAL_SYNDROME__OCNDS
OPITZ_KAVEGGIA_SYNDROME__OKS
OTITIS_MEDIA_SUSCEPTIBILITY_TO__OMS
OTOPALATODIGITAL_SYNDROME_TYPE_I__OPD1
O_DONNELL_LURIA_RODAN_SYNDROME__ODLURO
Oculocutaneous_albinism
Opitz_GBBB_syndrome
Orofaciodigital_syndrome
Osteogenesis_imperfecta
PFEIFFER_SYNDROME
PHELAN_MCDERMID_SYNDROME__PHMDS
PIERPONT_SYNDROME__PRPTS
POIKILODERMA_WITH_NEUTROPENIA__PN
PSMC5
Pontocerebellar_hypoplasia
RAUCH_STEINDL_SYNDROME__RAUST
RENPENNING_SYNDROME_1__RENS1
RETT_SYNDROME__RTT
ROBIN_SEQUENCE_WITH_CLEFT_MANDIBLE_AND_LIMB_ANOMALIES
Rothmund_Thomson_syndrome
SANDESTIG_STEFANOVA_SYNDROME__SANDSTEF
SAUL_WILSON_SYNDROME__SWILS
SCHUURS_HOEIJMAKERS_SYNDROME__SHMS
SHASHI_PENA_SYNDROME__SHAPNS
SHORT_STATURE_ONYCHODYSPLASIA_FACIAL_DYSMORPHISM_AND_HYPOTRICHOSIS__SOFT
SHORT_SYNDROME
SIMPSON_GOLABI_BEHMEL_SYNDROME_TYPE_1__SGBS1
SKRABAN_DEARDORFF_SYNDROME__SKDEAS
SMITH_KINGSMORE_SYNDROME__SKS
SNIJDERS_BLOK_CAMPEAU_SYNDROME__SNIBCPS
Seckel_syndrome
Short_stature_facial_dysmorphism_and_skeletal_anomalies_with_or_without_cardiac_anomalies
Silver_Russell_syndrome
Spinocerebellar_ataxia_autosomal_recessive
Stickler_syndrome
TAKENOUCHI_KOSAKI_SYNDROME__TKS
TCEAL1
TMEM147
TOLCHIN_LE_CAIGNEC_SYNDROME__TOLCAS
TURNPENNY_FRY_SYNDROME__TPFS
Teebi_hypertelorism_syndrome
Three_M_syndrome
Trichohepatoenteric_syndrome
VERHEIJ_SYNDROME__VRJS
VICI_SYNDROME__VICIS
WEISS_KRUSZKA_SYNDROME__WSKA
WITTEVEEN_KOLK_SYNDROME__WITKOS
WOLF_HIRSCHHORN_SYNDROME__WHS
Waardenburg_syndrome
XIA_GIBBS_SYNDROME__XIGIS
YOU_HOOVER_FONG_SYNDROME__YHFS
ZTTK_SYNDROME__ZTTKS
Zimmermann_Laband_syndrome
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LICENSE
CC BY 4.0 If you use this dataset in a research paper, please cite it using the following BibTeX:
@misc{
lessthan40multiplestepaug_dataset,
title = { lessthan40multiplestepaug Dataset },
type = { Open Source Dataset },
author = { geneticDisorders },
howpublished = { \url{ https://universe.roboflow.com/geneticdisorders/lessthan40multiplestepaug } },
url = { https://universe.roboflow.com/geneticdisorders/lessthan40multiplestepaug },
journal = { Roboflow Universe },
publisher = { Roboflow },
year = { 2024 },
month = { jul },
note = { visited on 2024-11-25 },
}