#Format: diseaseId<tab>gene-symbol<tab>gene-id(entrez)<tab>HPO-ID<tab>HPO-term-name
OMIM:201810	HSD3B2	3284	HP:0000037	Male pseudohermaphroditism
OMIM:201810	HSD3B2	3284	HP:0008221	Adrenal hyperplasia
OMIM:201810	HSD3B2	3284	HP:0000047	Hypospadias
OMIM:606070	MATR3	9782	HP:0001260	Dysarthria
OMIM:606070	MATR3	9782	HP:0003805	Rimmed vacuoles
OMIM:606070	MATR3	9782	HP:0002127	Abnormal upper motor neuron morphology
OMIM:606070	MATR3	9782	HP:0003828	Variable expressivity
OMIM:606070	MATR3	9782	HP:0003547	Shoulder girdle muscle weakness
OMIM:606070	MATR3	9782	HP:0000006	Autosomal dominant inheritance
OMIM:606070	MATR3	9782	HP:0002366	Abnormal lower motor neuron morphology
OMIM:606070	MATR3	9782	HP:0008756	Bowing of the vocal cords
OMIM:606070	MATR3	9782	HP:0001347	Hyperreflexia
OMIM:606070	MATR3	9782	HP:0007354	Amyotrophic lateral sclerosis
OMIM:606070	MATR3	9782	HP:0003236	Elevated serum creatine phosphokinase
OMIM:606070	MATR3	9782	HP:0002015	Dysphagia
OMIM:606070	MATR3	9782	HP:0002460	Distal muscle weakness
OMIM:606070	MATR3	9782	HP:0003581	Adult onset
OMIM:606070	MATR3	9782	HP:0000762	Decreased nerve conduction velocity
OMIM:606070	MATR3	9782	HP:0002835	Aspiration
OMIM:606070	MATR3	9782	HP:0001609	Hoarse voice
OMIM:606070	MATR3	9782	HP:0002747	Respiratory insufficiency due to muscle weakness
OMIM:606070	MATR3	9782	HP:0002483	Bulbar signs
OMIM:606070	MATR3	9782	HP:0001283	Bulbar palsy
OMIM:606070	MATR3	9782	HP:0001739	Abnormality of the nasopharynx