Arthritis, and Depressivity
Diseases related with Arthritis and Depressivity
In the following list you will find some of the most common rare diseases related to Arthritis and Depressivity that can help you solving undiagnosed cases.
Top matches:
Legg-Calve-Perthes disease (LCPD) is the term used to describe uni- or bilateral avascular necrosis (AVN) of the femoral head in children.
LEGG-CALVÉ-PERTHES DISEASE Is also known as legg-perthes disease|osteochondrosis of the capital femoral epiphysis|perthes disease|aseptic necrosis of the capital femoral epiphysis|lcp|osteochondritis of the capital femoral epiphysis
Related symptoms:
- Short stature
- Pain
- Skeletal muscle atrophy
- Abnormality of the dentition
- Depressivity
SOURCES:
ORPHANET
MESH
OMIM
MENDELIAN
More info about LEGG-CALVÉ-PERTHES DISEASE
Autosomal dominant dopa-responsive dystonia (DYT5a) is a rare neurometabolic disorder characterized by childhood-onset dystonia that shows a dramatic and sustained response to low doses of levodopa (L-dopa) and that may be associated with parkinsonism at an older age.
AUTOSOMAL DOMINANT DOPA-RESPONSIVE DYSTONIA Is also known as hpd with marked diurnal fluctuation|gtpch1-deficient dopa-responsive dystonia|gtpch1-deficient drd|dyt5a|hereditary progressive dystonia with marked diurnal fluctuation|autosomal dominant segawa syndrome
Related symptoms:
- Intellectual disability
- Hearing impairment
- Scoliosis
- Ataxia
- Hypertension
SOURCES:
ORPHANET
MENDELIAN
More info about AUTOSOMAL DOMINANT DOPA-RESPONSIVE DYSTONIA
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Other less relevant matches:
DYSTONIA, DOPA-RESPONSIVE; DRD Is also known as dystonia, progressive, with diurnal variation|dystonia 5|segawa syndrome, autosomal dominant|dystonia, dopa-responsive, autosomal dominant|dopa-responsive dystonia, autosomal dominant|dystonia-parkinsonism with diurnal fluctuation|dyt5
Related symptoms:
- Intellectual disability
- Hearing impairment
- Scoliosis
- Nystagmus
- Spasticity
SOURCES:
ORPHANET
OMIM
MENDELIAN
More info about DYSTONIA, DOPA-RESPONSIVE; DRD
Hereditary hypophosphatemic rickets with hypercalciuria (HHRH) is a hereditary renal phosphate-wasting disorder characterized by hypophosphatemia and hypercalciuria associated with rickets and/or osteomalacia.
HEREDITARY HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA Is also known as hypophosphatemia, x-linked|hpdr|hhrh|hyp|xlh|hypophosphatemic vitamin d-resistant rickets|vitamin d-resistant rickets, x-linked
Related symptoms:
- Short stature
- Hearing impairment
- Growth delay
- Neoplasm
- Sensorineural hearing impairment
SOURCES:
ORPHANET
OMIM
MENDELIAN
More info about HEREDITARY HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA
Juvenile Huntington disease (JHD) is a form of Huntington disease (HD; see this term), characterized by onset of signs and symptoms before 20 years of age.
JUVENILE HUNTINGTON DISEASE Is also known as huntington chorea|jhd|juvenile huntington chorea
Related symptoms:
- Seizures
- Ataxia
- Cognitive impairment
- Anemia
- Delayed speech and language development
SOURCES:
OMIM
ORPHANET
MENDELIAN
More info about JUVENILE HUNTINGTON DISEASE
Kniest dysplasia is a severe type II collagenopathy characterized by a short trunk and limbs, prominent joints and midface hypoplasia (round face with a flat nasal root).
Related symptoms:
- Short stature
- Hearing impairment
- Scoliosis
- Micrognathia
- Cleft palate
SOURCES:
OMIM
ORPHANET
MESH
MENDELIAN
More info about KNIEST DYSPLASIA
Giant cell arteritis (GCA) is a large vessel vasculitis predominantly involving the arteries originating from the aortic arch and especially the extracranial branches of the carotid arteries.
GIANT CELL ARTERITIS Is also known as horton disease|giant cell arteritis|temporal arteritis|cranial arteritis|polymyalgia rheumatica|gca
Related symptoms:
- Hearing impairment
- Ataxia
- Nystagmus
- Muscle weakness
- Ptosis
SOURCES:
OMIM
ORPHANET
MENDELIAN
More info about GIANT CELL ARTERITIS
Acromegaly is an acquired disorder related to excessive production of growth hormone (GH) and characterized by progressive somatic disfigurement (mainly involving the face and extremities) and systemic manifestations.
Related symptoms:
- Neoplasm
- Hypertension
- Fatigue
- Frontal bossing
- Abnormality of the dentition
SOURCES:
ORPHANET
MENDELIAN
More info about ACROMEGALY
Marshall syndrome is a malformation syndrome that is characterized by facial dysmorphism, severe hypoplasia of the nasal bones and frontal sinuses, ocular involvement, early-onset hearing loss, skeletal and anhidrotic ectodermal anomalies and short stature with spondyloepiphyseal dysplasia and early-onset osteoarthritis.
Related symptoms:
- Short stature
- Hearing impairment
- Hypertelorism
- Nystagmus
- Micrognathia
SOURCES:
MESH
OMIM
ORPHANET
MENDELIAN
More info about MARSHALL SYNDROME
Top 5 symptoms//phenotypes associated to Arthritis and Depressivity
Symptoms // Phenotype |
% cases |
Hearing impairment |
Common - Between 50% and 80% cases
|
Hypertension |
Uncommon - Between 30% and 50% cases
|
Arthralgia |
Uncommon - Between 30% and 50% cases
|
Osteoarthritis |
Uncommon - Between 30% and 50% cases
|
Short stature |
Uncommon - Between 30% and 50% cases
|
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Other less frequent symptoms
Patients with Arthritis and Depressivity. may also develop some of the following symptoms:
Uncommon Symptoms - Between 30% and 50% cases
Fatigue
Rheumatoid arthritis
Anxiety
Ataxia
Abnormality of the dentition
Frontal bossing
Bradykinesia
Scoliosis
Nystagmus
Gait ataxia
Rigidity
Hyperhidrosis
Myopia
Abnormality of the skeletal system
Gait disturbance
Obsessive-compulsive behavior
Rare Symptoms - Less than 30% cases
Abnormal cerebellum morphology
Tremor
Irritability
Hyperlordosis
Involuntary movements
Dystonia
Motor delay
Cerebral palsy
Neoplasm
Sensorineural hearing impairment
Behavioral abnormality
Paresis of extensor muscles of the big toe
Abnormality of movement
Muscle weakness
Hyperreflexia
Pain
Spinal canal stenosis
Conductive hearing impairment
Thick lower lip vermilion
Paresthesia
Visual impairment
Lens luxation
Hypoplastic ilia
Vitreoretinopathy
Ectopia lentis
Recurrent otitis media
High myopia
Retinal detachment
Platyspondyly
Joint stiffness
Proptosis
Diabetes mellitus
Glaucoma
Midface retrusion
Malar flattening
Short nose
Kyphosis
Depressed nasal bridge
Ptosis
Cataract
Transient hyperphenylalaninemia
Micrognathia
Cough
Weight loss
Abnormality of the substantia nigra
Cleft palate
Decreased CSF homovanillic acid
Hyperkinesis
Optic disc pallor
Fever
Anemia
Intellectual disability
Talipes equinovarus
Babinski sign
Seizures
Joint dislocation
Progressive flexion contractures
Pes cavus
Hypothyroidism
Sleep disturbance
Parkinsonism
Edema
Abnormality of extrapyramidal motor function
Focal dystonia
Lower limb hyperreflexia
Generalized dystonia
Brisk reflexes
Limb dystonia
Postural tremor
Impaired vibration sensation in the lower limbs
Torticollis
Horizontal nystagmus
Impaired mastication
Arteritis
Glossitis
Pericarditis
Gangrene
Gastrointestinal infarctions
Abdominal aortic aneurysm
Cerebral ischemia
Amaurosis fugax
Mediastinal lymphadenopathy
Abnormality of the pleura
Aortic dissection
Abnormal thrombocyte morphology
Arterial thrombosis
Recurrent pharyngitis
Double outlet right ventricle with subpulmonary ventricular septal defect without pulmonary stenosis
Visual field defect
Wide nose
Mitral regurgitation
Skeletal muscle atrophy
Migraine
Full cheeks
Macroglossia
Tapered finger
Long face
Retinal arteritis
Synophrys
Broad forehead
Hypertrophic cardiomyopathy
Coarse facial features
Macrotia
Mandibular prognathia
Jaw claudication
Elevated erythrocyte sedimentation rate
Diplopia
Diabetes insipidus
Enlarged joints
Visual loss
Headache
Renal insufficiency
Blindness
Optic atrophy
Peripheral neuropathy
Abnormal cartilage collagen
Alopecia
Flattened, squared-off epiphyses of tubular bones
Splayed epiphyses
Coronal cleft vertebrae
Enlarged thorax
Lumbar kyphoscoliosis
Dumbbell-shaped long bone
Arrhythmia
Congenital hip dislocation
Ophthalmoparesis
Sudden cardiac death
Vasculitis
Meningitis
Skin ulcer
Rhegmatogenous retinal detachment
Anorexia
Epistaxis
Hematuria
Abdominal pain
Hepatic failure
Vertigo
Thickened skin
Delayed skeletal maturation
Stroke
Myalgia
Aseptic necrosis
Tall stature
Large hands
Hoarse voice
Otitis media
Sparse eyelashes
Coxa valga
Sparse and thin eyebrow
Hypohidrosis
Amblyopia
Sparse scalp hair
Cerebral calcification
Esotropia
Thickened calvaria
Ectodermal dysplasia
Bifid uvula
Hypoplasia of the maxilla
Flat face
Genu valgum
Congenital cataract
Hypotrichosis
Sparse eyebrow
Aplasia cutis congenita
Brachycephaly
Abnormal vitreous humor morphology
Meningeal calcification
Small proximal tibial epiphyses
Wide tufts of distal phalanges
Irregular distal femoral epiphysis
Irregular proximal tibial epiphyses
Macrodontia of permanent maxillary central incisor
Calcification of falx cerebri
Hypoplastic frontal sinuses
Pierre-Robin sequence
Absent frontal sinuses
Ulnar bowing
Anhidrotic ectodermal dysplasia
Concave nasal ridge
Thick upper lip vermilion
Hypoplasia of the zygomatic bone
Radial bowing
Sparse hair
Long philtrum
Generalized hirsutism
Generalized hyperpigmentation
Dysuria
Abnormality of the endocrine system
Abnormal toenail morphology
Broad foot
Growth hormone excess
Joint swelling
Palpebral edema
Impotence
Deep palmar crease
Hypoplastic pelvis
Acne
Growth abnormality
Sleep apnea
Widely spaced teeth
Acanthosis nigricans
Abnormality of the fingernails
Neoplasm of the endocrine system
Anterior hypopituitarism
Anteverted nares
Abnormality of reproductive system physiology
Wide nasal bridge
Epicanthus
High palate
Low-set ears
Strabismus
Hypertelorism
Cortical diaphyseal thickening of the upper limbs
Broad jaw
Pheochromocytoma
Macrodactyly
Dysmenorrhea
Pituitary prolactin cell adenoma
Deep plantar creases
Galactorrhea
Hypersomnia
Paraganglioma
Long penis
Disproportionate short-trunk short stature
Spondyloepiphyseal dysplasia
Tracheal stenosis
Hyperphosphatemia
Fibular bowing
Hypocalciuria
Renal phosphate wasting
Hypophosphatemic rickets
Tetany
Elevated circulating parathyroid hormone level
Renal tubular dysfunction
Polyostotic fibrous dysplasia
Spinal cord compression
Ankylosis
Decreased serum iron
Osteomalacia
Glycosuria
Hyperparathyroidism
Tibial bowing
Hypomineralization of enamel
Pseudo-fractures
Hypophosphatemia
Cerebellar atrophy
Mental deterioration
Aggressive behavior
Decreased mean corpuscular volume
Hyperactivity
Epiretinal membrane
Myoclonus
Dementia
Ventriculomegaly
Trapezoidal distal femoral condyles
Dysphagia
Dysarthria
Delayed speech and language development
Cognitive impairment
Tertiary hyperparathyroidism
Shortening of the talar neck
Flattening of the talar dome
Femoral bowing
Bowing of the legs
Abnormality of the cerebral white matter
Dysphonia
Torsion dystonia
Upper motor neuron dysfunction
Hyperactive deep tendon reflexes
Resting tremor
Gaze-evoked nystagmus
Spastic diplegia
Confusion
Oromandibular dystonia
Paraplegia
Spastic paraplegia
Abnormal pyramidal sign
Difficulty walking
Encephalopathy
Hypertonia
Spasticity
Parkinsonism with favorable response to dopaminergic medication
Writer's cramp
Metaphyseal irregularity
Bone pain
Rickets
Hypercalcemia
Elevated alkaline phosphatase
Hypercalciuria
Abnormality of pelvic girdle bone morphology
Nephrocalcinosis
Hypocalcemia
Left ventricular hypertrophy
Axial dystonia
Ventricular hypertrophy
Ring scotoma
Photoreceptor layer loss on macular OCT
Growth delay
Fixed facial expression
Obsessive-compulsive trait
Infantile encephalopathy
Elliptocytosis
Abnormality of eye movement
Delayed epiphyseal ossification
Severe short stature
Hip dislocation
Retinopathy
Umbilical hernia
Skeletal dysplasia
Retrognathia
Pallor
Inguinal hernia
Micromelia
Nyctalopia
Abnormality of skin pigmentation
Retinal atrophy
Respiratory distress
Short neck
Macrocephaly
Anisocytosis
Global developmental delay
Round face
Macular edema
Short thorax
Lower limb asymmetry
Bell-shaped thorax
Glossoptosis
Tracheomalacia
Hip contracture
Arthropathy
Chorioretinal atrophy
Flared metaphysis
Cartilage destruction
Neonatal respiratory distress
Avascular necrosis of the capital femoral epiphysis
Coxa vara
Rhizomelia
Abnormality of epiphysis morphology
Abnormality of the metaphysis
Synovitis
Flexion contracture
Juvenile rheumatoid arthritis
Infertility
Type II diabetes mellitus
Slurred speech
Incoordination
Schizophrenia
Clumsiness
Broad-based gait
Progressive neurologic deterioration
Generalized-onset seizure
Akinesia
Neuronal loss in central nervous system
Brain atrophy
Chorea
Gliosis
Progressive cerebellar ataxia
Neurodegeneration
Falls
Personality changes
Hypokinesia
Poikilocytosis
Paranoia
Retinal pigment epithelial atrophy
Oral motor hypotonia
Frequent temper tantrums
Suicidal ideation
Neuronal loss in basal ganglia
Abnormal involuntary eye movements
Mania
Testicular atrophy
Muscle fibrillation
Dilated fourth ventricle
Chronic bronchitis
Head tremor
Upper limb undergrowth
Restlessness
Cerebellar vermis atrophy
Bronchitis
Small distal femoral epiphysis
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Frontal bossing and Nephrotic syndrome, related diseases and genetic alterations
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