| Diseases |
Alias |
|
| Interstitial Lung And Liver Disease |
|
Severe Early-Onset Pulmonary Alveolar Proteinosis Due To Mars Deficiency
|
ILLD
|
|
Pulmonary Alveolar Proteinosis, Reunion Island
|
Infantile Liver Failure Syndrome 2
|
|
Infantile Liver Failure Syndrome 2, Formerly
|
Ilfs2, Formerly
|
|
Hereditary Pulmonary Alveolar Proteinosis With Hepatic Involvement
|
Pap, Reunion Island Type
|
|
Pulmonary Alveolar Proteinosis, Reunion Island Type
|
Ilfs2
|
|
Lung And Liver Disease, Interstitial
|
|
|
| Charcot-Marie-Tooth Disease, Axonal, Type 2u |
|
CMT2U
|
Charcot-Marie-Tooth Disease Axonal Type 2u
|
|
Charcot-Marie-Tooth Neuropathy, Type 2u
|
Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2u
|
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2u
|
Autosomal Dominant Axonal Charcot-Marie-Tooth Disease Type 2u
|
|
Charcot-Marie-Tooth Neuropathy Type 2u
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due To Mars Mutation
|
|
Charcot-Marie-Tooth Disease 2u
|
|
|
| Trichothiodystrophy 9, Nonphotosensitive |
|
TTD9
|
Trichothiodystrophy 9, Non-Photosensitive
|
|
|
| Pulmonary Alveolar Proteinosis |
|
|
| Autosomal Recessive Spastic Paraplegia Type 70 |
|
|
| Charcot-Marie-Tooth Disease, Axonal, Type 2e |
|
Charcot-Marie-Tooth Disease Type 2
|
CMT2E
|
|
CMT2S
|
CMT2Y
|
|
Charcot-Marie-Tooth Disease Type 2e
|
Charcot-Marie-Tooth Disease Type 2y
|
|
Charcot-Marie-Tooth Disease Axonal Type 2s
|
Charcot-Marie-Tooth Disease, Axonal, Type 2s
|
|
Charcot-Marie-Tooth Disease, Type 2e
|
Hereditary Motor And Sensory Neuropathy Type 2
|
|
Charcot-Marie-Tooth Neuropathy, Type 2s
|
Charcot-Marie-Tooth Disease, Axonal, Autosomal Recessive, Type 2s
|
|
Charcot-Marie-Tooth Disease, Axonal, Type 2y
|
Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2y
|
|
Charcot-Marie-Tooth Neuropathy, Type 2y
|
Charcot-Marie-Tooth Disease, Type 2y
|
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2e
|
Charcot-Marie-Tooth Neuropathy Type 2e
|
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due To Vcp Mutation
|
Cmt2 Due To Vcp Mutation
|
|
Charcot-Marie-Tooth Disease Type 2s
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2
|
|
Autosomal Dominant Axonal Charcot-Marie-Tooth Disease
|
Cmt2
|
|
Charcot-Marie-Tooth Neuropathy, Type 2e
|
Hereditary Motor And Sensory Neuropathy Guadalajara Neuronal Type
|
|
Hereditary Motor And Sensory Neuropathy Okinawa Type
|
Autosomal Dominant Axonal Charcot-Marie-Tooth Type 2y
|
|
Charcot-Marie-Tooth Neuropathy Type 2y
|
Autosomal Recessive Axonal Charcot-Marie-Tooth Type 2s
|
|
Charcot-Marie-Tooth Neuropathy Type 2s
|
Charcot-Marie-Tooth Type 2
|
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2y
|
Charcot-Marie-Tooth Disease 2e
|
|
Charcot-Marie-Tooth Disease Axonal Type 2e
|
Charcot-Marie-Tooth Disease Neuronal Type 2e
|
|
Charcot-Marie-Tooth Disease 2s
|
Charcot-Marie-Tooth Neuropathy Axonal Type 2s
|
|
Charcot-Marie-Tooth Disease 2y
|
Charcot-Marie-Tooth Disease, Type 2
|
|
Hereditary Motor And Sensory-Neuropathy Type Ii
|
|
|
| Trichothiodystrophy |
|
Ttd
|
Amish Brittle Hair Syndrome
|
|
Bids Syndrome
|
Brittle Hair-Intellectual Impairment-Decreased Fertility-Short Stature Syndrome
|
|
Ibids
|
Pibids
|
|
Trichothiodystrophy Syndromes
|
|
|
| Infantile Liver Failure Syndrome 1 |
|
ILFS1
|
Acute Infantile Liver Failure-Multisystemic Involvement Syndrome
|
|
Liver Failure Syndrome, Infantile, Type 1
|
Liver Failure
|
|
|
| Charcot-Marie-Tooth Disease, Axonal, Type 2w |
|
CMT2W
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2w
|
|
Charcot-Marie-Tooth Neuropathy, Type 2w
|
Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2w
|
|
Charcot-Marie-Tooth Disease, Axonal Type 2w
|
Autosomal Dominant Axonal Charcot-Marie-Tooth Disease Type 2w
|
|
Charcot-Marie-Tooth Neuropathy Type 2w
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due To Hars Mutation
|
|
Charcot-Marie-Tooth Disease 2w
|
|
|
| Charcot-Marie-Tooth Disease |
|
Cmt
|
Hmsn
|
|
Hereditary Motor And Sensory Neuropathy
|
Pma
|
|
Cmt - Charcot-Marie-Tooth Disease
|
Charcot Marie Tooth Disease
|
|
Charcot-Marie-Tooth Hereditary Neuropathy
|
Charcot-Marie-Tooth Syndrome
|
|
Peroneal Muscular Atrophy
|
Hereditary Motor And Sensory Neuropathies
|
|
|
| Spastic Ataxia 3 |
|
|
| Charcot-Marie-Tooth Disease, Axonal, Type 2d |
|
Charcot-Marie-Tooth Disease Type 2d
|
CMT2D
|
|
Charcot-Marie-Tooth Disease, Type 2d
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2d
|
|
Charcot-Marie-Tooth Disease Neuronal Type 2d
|
Charcot-Marie-Tooth Neuropathy Type 2d
|
|
Charcot-Marie-Tooth Disease, Neuronal, Type 2d
|
Charcot-Marie-Tooth Neuropathy, Type 2d
|
|
Charcot-Marie-Tooth Disease 2d
|
Charcot-Marie-Tooth Disease Axonal Type 2d
|
|
|
| Tooth Disease |
|
Tooth Diseases
|
Teeth Disease
|
|
Tooth Disorders
|
|
|
| Charcot-Marie-Tooth Disease, Axonal, Type 2n |
|
Charcot-Marie-Tooth Disease Axonal Type 2n
|
CMT2N
|
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2n
|
Charcot-Marie-Tooth Neuropathy Axonal Type 2n
|
|
Charcot-Marie-Tooth Neuropathy, Axonal, Type 2n
|
Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2n
|
|
Autosomal Dominant Axonal Charcot-Marie-Tooth Disease Type 2n
|
Charcot-Marie-Tooth Disease 2n
|
|
Charcot-Marie-Tooth Disease Axonal Autosomal Dominant Type 2n
|
Charcot-Marie-Tooth Disease, Type 2n
|
|
|
| Usher Syndrome, Type Iiib |
|
Usher Syndrome Type 3b
|
USH3B
|
|
Usher Syndrome Type Iiib
|
Usher Syndrome 3b
|
|
|
| Charcot-Marie-Tooth Disease, Dominant Intermediate C |
|
CMTDIC
|
Charcot-Marie-Tooth Disease Dominant Intermediate C
|
|
Di-Cmtc
|
Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease Type C
|
|
Charcot-Marie-Tooth Neuropathy, Dominant Intermediate C
|
Charcot-Marie-Tooth Neuropathy Dominant Intermediate C
|
|
Charcot-Marie-Tooth Disease, Dominant, Intermediate Type, C
|
Charcot-Marie-Tooth Disease, Dominant Intermediate, Type C
|
|
|
| Spastic Ataxia 2 |
|
|
| Infantile Liver Failure Syndrome |
|
|
| Liver Disease |
|
Liver Failure
|
Liver Diseases
|
|
Abnormality Of The Liver
|
Liver Dysfunction
|
|
Disorder Of Liver
|
Hepatic Disorder
|
|
Hepatic Disease
|
Disease Of Bilirubin Metabolism
|
|
Disorder Of Bilirubin Metabolism
|
Liver Decompensation
|
|
Liver Function Failure
|
Hepatic Failure Nos
|
|
Liver Failure Nos
|
End Stage Liver Disease
|
|
Decompensated Liver Failure
|
Decompensation Of Liver Function
|
|
Hepatic Decompensation
|
Hepatic Insufficiency
|
|
Liver Cell Necrosis With Hepatic Failure
|
Liver Insufficiency
|
|
Decompensated Liver Disease
|
End Stage Liver Failure
|
|
Liver Necrosis With Hepatic Failure
|
|
|
| Charcot-Marie-Tooth Disease, Recessive Intermediate B |
|
Charcot-Marie-Tooth Disease Recessive Intermediate B
|
CMTRIB
|
|
Ri-Cmtb
|
Charcot-Marie-Tooth Disease, Recessive Intermediate, B
|
|
Autosomal Recessive Intermediate Charcot-Marie-Tooth Disease Type B
|
Charcot-Marie-Tooth Neuropathy Recessive Intermediate B
|
|
Charcot-Marie-Tooth Neuropathy, Recessive Intermediate B
|
Ri-Cmt Type B
|
|
Charcot-Marie-Tooth Disease, Recessive, Intermediate Type, B
|
|
|
| Aminoaciduria |
|
|
| Charcot-Marie-Tooth Disease Intermediate Type |
|
Intermediate Charcot-Marie-Tooth Disease
|
Charcot-Marie-Tooth Disease Dominant Intermediate
|
|
Charcot-Marie-Tooth Disease Recessive Intermediate
|
Intermediate Cmt
|
|
Intermediate Hereditary Motor And Sensory Neuropathy
|
Charcot-Marie-Tooth Disease, Intermediate Type
|
|
Charcot-Marie-Tooth, Intermediate
|
|
|
| Interstitial Lung Disease |
|
Ild
|
Lung Diseases, Interstitial
|
|
Lung Diseases Interstitial
|
Interstitial Lung Diseases
|
|
|
| Mehmo Syndrome |
|
Mental Retardation, Epileptic Seizures, Hypogonadism And Hypogenitalism, Microcephaly, And Obesity
|
MEHMO
|
|
Mrxs20
|
Mrxs25
|
|
X-Linked Intellectual Disability-Epileptic Seizures-Hypogenitalism-Microcephaly-Obesity Syndrome
|
Mrxsbrk
|
|
Mental Retardation, X-Linked, Syndromic 20
|
Mental Retardation, X-Linked, Syndromic 25
|
|
Mental Retardation, X-Linked, Syndromic, Borck Type
|
Syndromic X-Linked Mental Retardation 20
|
|
Syndromic X-Linked Mental Retardation 25
|
Intellectual Disability, Epileptic Seizures, Hypogonadism And Hypogenitalism, Microcephaly, And Obesity
|
|
X-Linked Mehmo Syndrome
|
|
|
| Motor Neuron Disease |
|
Anterior Horn Cell Disease
|
Motor Neuron Diseases
|
|
Mnd - [Motor Neurone Disease]
|
Lou Gehrig Disease
|
|
Creeping Palsy
|
Creeping Paralysis
|
|
Bulbar Motor Neuron Disease
|
Bulbar Syndrome
|
|
Anterior Horn Cell Disorder
|
Hereditary Motor Neuron Disease
|
|
|
| Lactic Acidosis |
|
Acidosis, Lactic
|
Acidosis Lactic
|
|
|
| Autosomal Dominant Distal Hereditary Motor Neuronopathy |
|
Autosomal Dominant Distal Hereditary Motor Neuropathy
|
Autosomal Dominant Dhmn
|
|
Autosomal Dominant Distal Spinal Muscular Atrophy
|
|
|
| Arthrogryposis, Distal, Type 1a |
|
Distal Arthrogryposis Type 1
|
Digitotalar Dysmorphism
|
|
DA1A
|
Da1
|
|
Amcd1
|
Arthrogryposis, Distal, Type 2b4
|
|
Distal Arthrogryposis Type 1a
|
Arthrogryposis, Distal, Type 1
|
|
Arthrogryposis Multiplex Congenita Distal Type 1
|
Arthrogryposis Multiplex Congenita, Distal Type 1
|
|
Arthrogryposis Multiplex Congenita, Distal, Type I
|
Distal Arthrogryposis Type 1b
|
|
Arthrogryposis, Distal, 1a
|
Amc
|
|
Arthrogryposis Multiplex Congenita
|
Arthrogryposis, Distal, 2b4
|
|
DA2B4
|
Arthrogryposis Multiplex Congenita, Distal, Type 1
|
|
Arthrogryposis
|
|
|
| Neuronopathy, Distal Hereditary Motor, Type Va |
|
Dsmav
|
Distal Hereditary Motor Neuropathy Type V
|
|
Young Adult-Onset Distal Hereditary Motor Neuropathy
|
Neuronopathy, Distal Hereditary Motor, Type V
|
|
Distal Hereditary Motor Neuronopathy Type 5
|
Dhmn5
|
|
Distal Spinal Muscular Atrophy Type 5
|
HMN5A
|
|
Hmn5
|
Dhmn5a
|
|
Dhmn Va
|
Dsmava
|
|
Spinal Muscular Atrophy, Distal, With Upper Limb Predominance
|
Distal Hmn V
|
|
Autosomal Recessive Distal Spinal Muscular Atrophy Type 5
|
Dsma5
|
|
Young Adult-Onset Dhmn
|
Dhmn-V
|
|
Hmn V
|
Neuronopathy, Distal Hereditary Motor, Type 5a
|
|
Hmn 5a
|
Neuropathy, Distal Hereditary Motor, Type Va
|
|
Spinal Muscular Atrophy, Distal, Type Va
|
Spinal Muscular Atrophy, Distal, Type V
|
|
Distal Spinal Muscular Atrophy Type V
|
Distal Spinal Muscular Atrophy With Upper Limb Predominance
|
|
Distal Hereditary Motor Neuronopathy Type 5a
|
Distal Hmn Va
|
|
Distal Spinal Muscular Atrophy Type Va
|
Distal Hereditary Motor Neuropathy, Type V
|
|
Distal Hereditary Motor Neuronopathy, Type V
|
Distal Spinal Muscular Atrophy, Type V
|
|
Spinal Muscular Atrophy, Distal Type V
|
Distal Hereditary Motor Neuropathy Type 5
|
|
Neuronopathy, Distal Hereditary Motor, 5a
|
Dhmn V
|
|
Distal Hereditary Motor Neuronopathy Type Va
|
Distal Hereditary Motor Neuropathy Type Va
|
|
Dsma-V
|
Hmn Va
|
|
Spinal Muscular Atrophy Distal Type V
|
Spinal Muscular Atrophy Distal Type Va
|
|
Spinal Muscular Atrophy Distal With Upper Limb Predominance
|
Neuropathy, Distal Hereditary Motor, Type V
|
|
Neuropathy, Motor, Distal, Hereditary, Type Va
|
|
|
| Sleeping Sickness |
|
African Trypanosomiasis
|
African Sleeping Sickness
|
|
Trypanosomiasis, Human East-African
|
Trypanosomiasis, East African
|
|
Trypanosomiasis African
|
Trypanosomiasis, African
|
|
Human African Trypanosomiasis
|
|
|
| Microcephaly |
|
Microencephaly
|
Microcephalus
|
|
Microcephalic
|
Nanocephaly
|
|
Congenital Microcephaly
|
Brain Hypoplasia
|
|
Brain Nondevelopment
|
Cephalic Hypoplasia
|
|
Undeveloped Cerebrum
|
Undeveloped Brain
|
|
Micrencephalon
|
Micrencephaly
|
|
|
